Infertility

145

Review clinical trials related to Infertility. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Ovarian Stromal Stiffness and Ovarian Reserve Parameters Via Transvaginal Shear Wave Elastography

This study aims to evaluate the relationship between ovarian stromal stiffness measured by transvaginal shear wave elastography (SWE) and conventional hormonal and ultrasonographic parameters of ovarian reserve. Reproductive-aged female patients will be evaluated to determine whether tissue elasticity provided by SWE correlates with ovarian function markers such as anti-Müllerian hormone (AMH), antral follicle count (AFC), and ovarian volume.

Participants needed: 100
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri Universitesi Gazi Yasargil Training and Research HospitalUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Female patients aged 18 to 45 years. [+3]

History of prior ovarian or adnexal surgery. [+5]

Status: Recruiting

Association Between Peri-Transfer Endometrial Peristalsis And Live Birth In Modified Natural Cycle Frozen Embryo Transfer: A Prospective Cohort Study

The uterus is a dynamic muscular organ that undergoes rhythmic, wave-like contractions known as endometrial peristalsis or endometrial waves. This muscular activity, which is an essential component of natural fertility, presents a nuanced and sometimes contradictory role in the context of assisted reproductive treatments. Endometrial peristalsis refers to the frequency, amplitude, and pattern of myometrial contractions occurring in different reproductive phases. These peristalsis play vital roles in sperm transport, embryo migration, and implantation. Clinical and imaging studies suggest that abnormal patterns or excessive contractility at the time of embryo transfer may disrupt endometrial-embryo synchrony, impair implantation, and increase miscarriage risk. However, most evidence on endometrial peristalsis pertains to fresh embryo transfer cycles, natural conceptions, or pathological contexts, such as adenomyosis or fibroids, with limited insights regarding its effects on different endometrial preparation protocols in frozen embryo transfer (FET). Understanding the dynamics of endometrial peristalsis in this context is clinically important, as inappropriate contractile activity could physically expel the embryo or create a non-receptive environment, ultimately reducing the chances of live birth. Despite its theoretical significance, there is a paucity of robust, prospective data correlating endometrial peristalsis patterns measured around the time of FET with different endometrial preparation protocols with subsequent pregnancy outcomes.

Participants needed: 384
Trial details
Age: 18-42Biological sex: FemaleType: ObservationalSponsor: Mỹ Đức HospitalUpdated: Aug 19, 2026Locations: 2
Eligibility criteria

Women aged 18 - 42 years old [+2]

Having an allergy and contraindications for exogenous hormone administration (e.... [+5]

Status: Recruiting

Biorepository in Participants Who Undergo OTC for Gonadotoxic Therapy

Background: Medical advances have improved survival rates for many cancers and other illnesses. This means that more people are coping with the long-term effects of these treatments. Some treatments can cause female infertility. Ovarian tissue cryopreservation (OTC) may help. Before undergoing a treatment that may damage their fertility, patients may opt to freeze a sample of ovarian tissue. The tissue contains immature egg cells. When thawed, the tissue can be reimplanted. This procedure can help women become pregnant. Objective: This natural history study will create a databank of ovarian tissue. The NIH will provide OTC as a clinical service. The NIH will also request a portion of the tissue to use for research. Eligibility: Females aged 4 to 35 who opt to have OTC before receiving cancer treatment. Design: Participants will be screened. Their existing medical records will be reviewed. They will be asked if they want to donate a portion of their ovarian tissue for research. No more than 20% of the tissue collected will be taken for research. Some other tissues that would otherwise be discarded will also be kept. Medical data from each participant may also be collected and stored in the database. This data may include results of routine blood tests, imaging tests, and other information. The data will be coded for privacy. Participants will answer a questionnaire. They will be asked about their fertility treatment and general health. The survey takes about 30 minutes. They will repeat the questionnaire once a year for 30 years. ...

Participants needed: 100
Trial details
Age: 4-35Biological sex: FemaleType: ObservationalSponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Updated: Aug 18, 2026Locations: 1
Eligibility criteria

Provision of signed and dated informed consent/assent form. [+2]

Status: Recruiting

Non-Euploid Embryo Transfer (NEET) Registry

The NEET Registry is a registry to track and study the outcomes of non-euploid embryo transfers (NEET) in The Prelude Network

Participants needed: 1,000
Trial details
Biological sex: FemaleType: ObservationalSponsor: Inception Fertility Research Institute, LLCUpdated: Aug 14, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Patient is planning a non-euploid embryo transfer (NEET) at a fertility clinic i... [+1]

Not applicable

Status: Recruiting

A Study to Compare the Efficacy and Safety of Follitropin Alfa/Lutropin Alfa Versus hMG in Japanese Participants With LH and FSH Deficiency Undergoing ART (HINATA)

The purpose of this study is to assess the efficacy and safety of follitropin alfa/lutropin alfa in Japanese participants with Luteinizing hormone (LH) and Follicle stimulating hormone (FSH) deficiency undergoing Assisted reproductive technology (ART). The study duration is approximately 5.5 months for nonpregnant participants and 13 months for participants with confirmed pregnancy in Part A.

Participants needed: 266
Trial details
Phase: Phase 3Age: 18-42Biological sex: FemaleType: InterventionalSponsor: Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, GermanyUpdated: Aug 10, 2026Locations: 21
Eligibility criteria

Participants who are premenopausal wishing to conceive [+7]

Participants with history of severe OHSS in any previous ovarian stimulation cyc... [+5]

Status: Recruiting

The Hysterosalpingogram (HSG) Experience And Tubal Spasm (HEAT) Study

The hysterosalpingogram (HSG) is the gold standard of assessing fallopian tube patency and involves the placement of a transcervical catheter to allow for instillation of radio-opaque dye into the uterine cavity and fallopian tubes which are then imaged with abdominal x-ray. A common side effect of the instillation of dye is the uterine cramping, which is both uncomfortable for the patient as well as can cause iatrogenic proximal occlusion of the fallopian tubes. Proximal tubal obstruction is often not representative of true tubal obstruction but is rather an artifact of the test. Prior studies measuring the perceived pain and cramping during HSG have been conducted which have shown reduced pain scores and decreased uterine cramping when warmed contrast dye is used. The researchers propose that the use of warmed contrast media during HSG will be correlated with decreased pain scores and fewer cases of proximal tubal occlusion in women with otherwise normal uterine anatomy.

Participants needed: 240
Trial details
Phase: Early Phase 1Age: 18-45Biological sex: FemaleType: InterventionalSponsor: University of OklahomaUpdated: Jul 30, 2026Locations: 1
Eligibility criteria

History of fibroids [+9]

Status: Not yet recruiting

Progesterone Luteal Support in Unexplained Infertility Management

The purpose of this study is to evaluate whether progesterone in women with unexplained infertility can increases live birth rate. The main research question is: Does luteal phase support with progesterone increase the live birth rate among couples with unexplained infertility? The study compares progesterone with placebo to determine the effectiveness of progesterone in unexplained infertility. Study participants will: * Perform home ovulation tests and maintain a digital diary to record menstrual cycles and study medication use.10 * Take progesterone or placebo twice daily during the luteal phase of each menstrual cycle for up to six months.11 * Continue usual medical care. No additional hospital visits or invasive procedures are required as part of the study.

Participants needed: 640
Trial details
Phase: Phase 3Age: 18-43Biological sex: FemaleType: InterventionalSponsor: Simone BroerUpdated: Jul 30, 2026
Eligibility criteria

Primary or secondary infertility for at least a period of 1 year Participants wh... [+8]

Uncorrected uterine factors, such as endometrial polyps or submucosal fibroids, [+4]

Status: Recruiting

Inherited Reproductive Disorders

Background: \- During puberty, children begin to develop into adults. Problems with the hormones released during puberty can affect the reproductive system. Some people have low hormone levels that severely delay or prevent puberty. Others start puberty abnormally early. Other people may have a normal puberty but develop reproductive disorders later in life. Researchers want to study people with reproductive disorders to learn more about how these disorders may be inherited. Objectives: \- To learn how reproductive system disorders may be inherited. Eligibility: * People with one of the following problems: * Abnormally early puberty * Abnormally late or no puberty * Normal puberty with hormonal problems that develop later in life * People who have not yet had puberty but have symptoms that indicate low hormone levels. Design: * Participants will provide a blood sample for testing. They will complete a questionnaire about their symptoms. They will also have a scratch-and-sniff test to study any problems with their ability to smell. * Participant medical records will be reviewed. Participants will also provide a family medical history. * Family members of those in the study may be invited to participate. * Treatment will not be provided as part of this study.

Participants needed: 850
Trial details
Age: 6-120Biological sex: AllType: ObservationalSponsor: National Institute of Environmental Health Sciences (NIEHS)Updated: Jul 28, 2026Locations: 2
Eligibility criteria

failure to go through a normal, age-appropriate, spontaneous puberty and low sex... [+4]

Patients who have additional pituitary deficiencies, effectively ruling out isol... [+1]

Status: Not yet recruiting

Patient Empowerment Project (PEP) Study

The Patient Empowerment Project (PEP) will be integrated into the intake process at a fertility clinic to prepare clinical staff for any patient sensitivities or preferences and provide extra support if needed. The study will evaluate if the PEP increases patient retention and patient satisfaction scores.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: Inception Fertility Research Institute, LLCUpdated: Jul 27, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Endometrial Peristalsis and Pregnancy Outcomes in Hormone Replacement Therapy (HRT) - Frozen Embryo Transfer (FET) Cycles

Endometrial peristalsis may influence embryo implantation and pregnancy outcomes, but its role during hormone replacement therapy (HRT)-prepared frozen embryo transfer (FET) cycles remains unclear. This prospective observational study will assess endometrial peristalsis at predefined time points during HRT-prepared FET cycles using transvaginal ultrasonography and evaluate its association with pregnancy outcomes. The study aims to clarify the clinical significance of endometrial peristalsis in HRT-prepared FET cycles and to provide evidence supporting endometrial assessment in assisted reproductive technology.

Participants needed: 442
Trial details
Age: 18-42Biological sex: FemaleType: ObservationalSponsor: Mỹ Đức HospitalUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

Women aged 18 - 42 years old [+3]

Having an allergy and contraindications for exogenous hormone administration (e.... [+4]

Status: Recruiting

Food Intake Among Women and Men in Fertility Treatment

Worldwide infertility is highly prevalent and lifestyle factors, such as food intake, could have an essential role in the success of a fertility treatment. The literature is not consistent and adequate for recommendations to the increasing number of women and men of reproductive age who ask for lifestyle guidance. Therefore, the aims of the Food \& Fertility study will be to investigate the association between food intake and semen quality, pregnancy- and live birth rates in women and men undergoing assisted reproductive technology (ART) treatment.

Participants needed: 4,000
Trial details
Biological sex: AllType: ObservationalSponsor: Aalborg University HospitalUpdated: Jul 8, 2026Locations: 8Duration: 10 Months
Eligibility criteria

Women and men undergoing fertility treatment: in vitro fertilization (IVF), intr... [+2]

Treatment with double donation (both semen and oocyte donation)

Status: Recruiting

GnRH for Luteal Support in IVF/ICSI/FET Cycles

During IVF cycles an embryo is generally placed into the uterine cavity between 3 and 5 days after fertilization. For a successful pregnancy to take place, that embryo must then implant in the properly primed and staged endometrium, which subsequently must continue to develop to accommodate the growing and maturing embryo and then fetus. This process is normally regulated by hormonal interactions between the fetal, endometrial and luteal tissue. It has been found that after IVF additional support for the endometrium with progesterone improves implantation and subsequent live birth rates in IVF cycle . Recent data has shown that additional supplementation with a single administration of a GnRH agonist around the time the time of embryo transfer may further enhance these rates .

Participants needed: 350
Trial details
Phase: Phase 4Age: 18-40Biological sex: FemaleType: InterventionalSponsor: University Reproductive AssociatesUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

women undergoing IVF/ICSI or frozen embryo transfers (FET) that less than 40 yea...

day 3 transfers

Status: Recruiting

Ultra-Long GnRH-a Pretreatment for FET Outcomes in Patients With Deep Infiltrating Endometriosis

Deep infiltrating endometriosis is a severe form of endometriosis that may reduce fertility and negatively affect pregnancy outcomes after assisted reproductive treatment. Gonadotropin-releasing hormone agonist pretreatment may suppress endometriotic lesions, reduce inflammation, and improve endometrial receptivity, but its benefit before frozen-thawed embryo transfer remains uncertain. This randomized controlled study will evaluate whether ultra-long GnRH-a pretreatment before hormone replacement therapy improves clinical pregnancy outcomes in patients with deep infiltrating endometriosis undergoing their first frozen-thawed embryo transfer cycle. Eligible participants will be randomly assigned to either the GnRH-a pretreatment group or the control group. Participants in the GnRH-a group will receive two injections of long-acting GnRH-a before hormone replacement therapy for endometrial preparation, while participants in the control group will receive routine hormone replacement therapy alone. The primary outcome is clinical pregnancy rate, defined as the presence of a gestational sac on transvaginal ultrasound 30 ± 3 days after embryo transfer. Secondary outcomes include implantation rate, ectopic pregnancy rate, early spontaneous abortion rate, ongoing pregnancy rate at 12 weeks of gestation, and delivery rate. Safety will be evaluated by recording adverse events after GnRH-a injection. The planned enrollment is 120 participants.

Participants needed: 120
Trial details
Phase: Phase 4Age: 18-39Biological sex: FemaleType: InterventionalSponsor: Li-jun DingUpdated: Jul 10, 2026Locations: 1
Eligibility criteria

Female patients aged 18 to 39 years. [+4]

Abnormal chromosomal karyotype. [+6]

Status: Recruiting

Automation of the In Vitro Fertilization Laboratory

Enrolled patients will undergo an Assisted Reproductive technology (ART) treatment using intracytoplasmic sperm injection (ICSI, the direct injection of a single sperm cell into an oocyte) as the method of insemination. In this prospective cohort study, patients' sperm, eggs, and embryos will be processed using an automated system called AURA (Conceivable Life Sciences), which consists of five subsystems. Specifically, sperm samples will be prepared for fertilization using the subsystem C:SPERM. Cumulus-oocyte complexes (COCs) containing the oocytes will be isolated from follicular fluid using the subsystem C:EGG. One out of every four COCs will be removed from the AURA system at random and processed according to the local treatment clinic's standard operating procedure. All other COCs will continue automated procedures and will be denuded, fertilized, incubated, and vitrified using the AURA subsystems C:EGG. C:ICSI, C:CULTURE and C:VIT, respectively. All automated procedures will be conducted under the supervision of a laboratory manager, who can intervene, address any potential anomalies, and override any steps undertaken by the automated AURA system. The study aims to deliver a descriptive evaluation of the AURA system, including assessing the device's performance, defined by its level of automation, efficiency, and throughput. As a secondary objective, the study aims to characterize the clinical performance of each of AURA's subsystems and correlate this performance against pre-established benchmarks in a non-inferiority statistical analysis. Finally, the study seeks to collect technical data related to AURA's hardware and software operation.

Participants needed: 150
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Conceivable Life SciencesUpdated: Jul 6, 2026Locations: 2
Eligibility criteria

Informed consent signed by the patients before treatment. [+5]

Patients diagnosed with recurrent pregnancy loss. [+15]

Status: Not yet recruiting

Embryo QUAlity in Ovarian Stimulation With hMG.

Ovarian stimulation (OS) is a key component of IVF, aimed at increasing oocyte yield and improving embryo development potential. While early protocols relied solely on FSH, newer approaches incorporate hMG and LH-based stimulation, allowing more individualized treatments for specific patient populations. Evidence suggests that hMG and recombinant FSH (rFSH) have comparable effectiveness in stimulation outcomes, and current guidelines support the use of both. However, the impact of different gonadotropins on embryo quality remains unclear, with mixed findings across protocols. Given the increasing use of combined rFSH and hMG and the limited data in PPOS protocols, this study proposes a randomized controlled trial to compare embryo quality between two different rFSH-hMG dosing strategies.

Participants needed: 240
Trial details
Phase: Phase 4Age: 38-41Biological sex: FemaleType: InterventionalSponsor: Fundacion DexeusUpdated: Jul 8, 2026Locations: 4
Eligibility criteria

Undergoing preimplantation genetic screening cycles [+3]

Previous poor ovarian response (≤3 oocytes with a conventional stimulation proto... [+7]

Status: Recruiting

Ultra-rapid Blastocyst Vitrification: Pilot Randomized Study

Blastocyst vitrification is standard in assisted reproduction, but clinical data on ultra-rapid vitrification are limited. This pilot study evaluates the safety, feasibility, and preliminary clinical performance of an ultra-rapid blastocyst vitrification protocol compared with the standard approach.

Participants needed: 80
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Fundacion DexeusUpdated: Jun 30, 2026Locations: 2
Eligibility criteria

Recipients of donor oocytes [+1]

Cycles involving PGT [+1]

Status: Not yet recruiting

Effect of Varicocelectomy on Spermatogenic Cell Count and Semen Parameters

This study aims to evaluate how varicocele surgery (varicocelectomy) affects the number of immature sperm cells (spermatogenic cells) found in the semen of infertile men. Varicocele, an abnormal dilation of veins in the scrotum, is a common cause of male infertility that can negatively impact semen quality and overall testicular function. While surgery is widely performed to improve standard semen parameters, this study specifically investigates its impact on the shedding of immature germ cells into the seminal fluid, which can be an indicator of impaired sperm production. Researchers will enroll 40 infertile married men, aged 20 to 45, who have been diagnosed with a clinical varicocele and exhibit abnormal semen parameters. All participants will undergo a single surgical intervention known as a subinguinal microsurgical varicocelectomy. To measure the effects of the surgery, participants will undergo careful semen analysis before the procedure, and again at 3 and 6 months postoperatively. The primary goal is to track changes in the spermatogenic cell count and abnormal sperm morphology, and to explore how these changes correlate with conventional semen parameters like sperm concentration, motility, and vitality.

Participants needed: 40
Trial details
Age: 20-45Biological sex: MaleType: InterventionalSponsor: Assiut UniversityUpdated: Jul 6, 2026
Eligibility criteria

Infertile married males diagnosed with clinical varicocele. [+3]

Azoospermic patients (complete absence of sperm in semen). [+7]

Status: Not yet recruiting

Safety Evaluation of the HyperSperm Sperm Preparation Procedure for In Vitro Fertilization

Prospective, multicenter, randomized clinical study evaluating the safety of a novel sperm preparation method for in vitro fertilization (IVF), compared to standard sperm preparation procedures.

Participants needed: 202
Trial details
Age: 20-45Biological sex: AllType: InterventionalSponsor: Fecundis Lab SLUpdated: Jun 26, 2026Locations: 2
Eligibility criteria

Couples undergoing in vitro fertilization (IVF) treatment. [+7]

Active sexually transmitted infection (STI). [+6]

Status: Not yet recruiting

Outcomes of Embryos Created From Abnormally Fertilized Oocytes

The purpose of this study is to retrospectively analyze data from multiple clinics in a fertility network on embryos that were created from abnormally fertilized oocytes (AFO) including the rate of transfers and any clinical outcomes in order to inform providers in their decision making regarding AFOs.

Participants needed: 92
Trial details
Biological sex: FemaleType: ObservationalSponsor: Inception Fertility Research Institute, LLCUpdated: Jun 24, 2026
Eligibility criteria

Underwent in vitro fertilization which resulted in a blastocyst derived from an...

Status: Recruiting

Hyaluronan-enriched Medium and Euploid Blastocyst Transfers

It has been proposed that enriching transfer media with hyaluronan (EmbryoGlue medium) improves pregnancy outcomes compared with media containing lower concentrations of this molecule. However, none of previous studies included preimplantation genetic testing for aneuploidy (PGT-A) embryos. In order to investigate the impact of this hyaluronan-enriched on pregnancy outcomes, it is essential to evaluate its efficacy on euploid-only embryo transfers. The aim of the present study is to evaluate whether a short period of exposure of euploid blastocysts to EmbryoGlue prior to and during transfer positively impact on pregnancy outcomes of frozen embryo transfer (FET) cycles.

Participants needed: 783
Trial details
Age: 18-46Biological sex: FemaleType: InterventionalSponsor: ART Fertility Clinics LLCUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

All frozen embryo transfer (FET) cycles with euploid blastocysts biopsied and vi... [+6]

FET cycles with preimplantation genetic testing for monogenic disorders (PGT-M)... [+5]

Status: Not yet recruiting

Effects of Visceral Osteopathic Massage on Semen Parameters and Hemodynamics Factors in Varicocele

The project aims to evaluate the effects of a visceral osteopathic manual therapy (VOM) protocol on semen parameters and testicular hemodynamic indicators in men diagnosed with varicocele. Varicocele, the most common correctable cause of male infertility, is a progressive vascular pathology characterized by dilation of the pampiniform plexus veins and venous reflux. Multifactorial mechanisms such as venous valve insufficiency, increased intra-abdominal pressure, microcirculatory impairment, and oxidative stress play a role in the pathophysiology of varicocele. Therefore, the present study investigates the clinical effectiveness of a non-invasive rehabilitation approach aimed at regulating intra-abdominal pressure and improving pelvic venous drainage. The study will be conducted using a prospective, randomized controlled clinical design, including male participants aged 18-45 years diagnosed with varicocele. The intervention group will receive visceral osteopathic manual therapy techniques two times per week for eight weeks, while the control group will receive lifestyle recommendations only. Before and after the intervention, semen analysis results, sperm morphology, motility parameters, and testicular venous hemodynamic measurements obtained by color Doppler ultrasonography will be compared. Parametric and non-parametric statistical methods will be used in the analyses. This project aims to generate clinical evidence regarding conservative, complementary medicine-based treatment options in the field of male infertility. Compared to studies on female reproductive health, research focusing on male reproductive health is more limited; therefore, this study is expected to contribute to the literature in this area. The results are anticipated to support the development of a cost-effective and accessible model for infertility treatment processes. In addition, the project aims to provide scientific data for the development of sustainable reproductive health approaches in terms of health economics in Türkiye. The study seeks to determine the effects of visceral osteopathic manual therapy on varicocele-related semen parameters and hemodynamic variables and to contribute to the development of new evidence-based approaches in the management of male infertility.

Participants needed: 32
Trial details
Age: 18-45Biological sex: MaleType: InterventionalSponsor: Ankara Yildirim Beyazıt UniversityUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Male individuals aged 18-45 years. [+5]

History of prior inguinal or scrotal surgery. [+8]

Status: Recruiting

IntelliWell: An AI-Assisted Imaging Platform for Detection and Location of Ultra-Rare Testicular Sperm in Surgical Specimens

This study will help determine whether an AI-assisted microwell platform (IntelliWell) can identify rare sperm cells in testicular samples found to not have sperm by conventional analysis. Instead of discarding testicular tissue which was found to be non-sperm bearing by conventional analysis the testicular tissue will be processed using IntelliWell and, if sperm is found and verified by embryologists, it may be used for intracytoplasmic sperm injection (ICSI).

Participants needed: 20
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Male subjects presenting to Brigham and Women's or Faulkner urology clinic with... [+2]

Status: Recruiting

A Large-scale, Prospective Cohort Study Was Conducted to Explore the Association Between Environmental Exposure and Behavioral Factors and Infertility (the Success Rate of Assisted Reproductive Technology)

The aim is to explore the reasons for the failure of assisted reproductive technology (ART) in infertile patients in Hunan Province and seek ways to improve the success rate of ART. The study will focus on how environmental exposure (such as environmental pollutants related to plastic products) and lifestyle and social factors affect the success rate of ART in infertile patients. In order to explore these issues in depth, the study plans to collect 5,000 samples (male: female ratio 1:1), screen the research subjects from infertile patients who visited Xiangya Third Hospital in Changsha, Hunan Province, and establish a large-scale, prospective infertility patient cohort. By collecting multi-faceted information of the research subjects, including sociodemographic characteristics, lifestyle, basic health status, etc., and conducting long-term follow-up observations, the ART live birth situation of infertile patients is analyzed. In terms of research methods, a multivariate analysis method will be used to explore the association between various factors and ART success rate, and a risk prediction model will be constructed. In addition, the study also hopes to clarify the specific reasons for the failure of infertile patients to receive ART, provide a scientific basis for clinical decision-making, and provide guidance for the formulation of environmental protection policies and the improvement of public reproductive health literacy. In general, this study, through a large-scale, prospective cohort study, deeply explores the various factors that affect the success rate of ART in infertile patients, and strives to build a risk prediction model in order to improve the success rate of ART and bring more hope to infertile families.

Participants needed: 5,000
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: The Third Xiangya Hospital of Central South UniversityUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

1. Women aged 18 to 46 who use their own eggs or men aged 18 to 55 who use their...

1. Artificial insemination population with any of the following ARTs contraindic...

Status: Not yet recruiting

Theta Healing-Based Intervention in Women With Polycystic Ovary Syndrome

This randomized controlled study aims to evaluate the effect of a Theta Healing-based intervention on fertility concerns, self-compassion, and body image in women diagnosed with Polycystic Ovary Syndrome (PCOS). Participants will be randomly assigned to intervention and control groups. The intervention group will receive a structured 5-day Theta Healing-based online intervention program, while the control group will continue routine care. Outcome measures will be assessed at baseline and 6 weeks after the intervention.

Participants needed: 142
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Ankara Medipol UniversityUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Women aged 18-45 years [+4]

Diagnosed psychiatric disorder [+3]

Status: Recruiting

Fertility Preservation Using Tamoxifen and Letrozole in Estrogen Sensitive Tumors Trial

Latrogenic infertility as a result of cancer treatment has a profound effect on long-term quality of life in survivors of reproductive-age cancers. Oocyte cryopreservation prior to cancer treatment has been associated with improved quality of life, with a potential ability to reduce long-term decision-related regret in cancer survivors. Though letrozole plus gonadotropin and and tamoxifen plus gonadotropin are currently routinely used worldwide in ovarian stimulation cycles for fertility preservation in patients with estrogen-receptor-positive breast cancer, it is not clear which of the two might lead to improved oocyte yield. Improved knowledge about the efficacy of these medications, with regard to oocyte yield, has the potential to significantly improve quality of life in reproductive-age breast cancer survivors.

Participants needed: 309
Trial details
Phase: Phase 3Age: 18-50Biological sex: FemaleType: InterventionalSponsor: University of California, San FranciscoUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

New breast cancer diagnosis [+3]

Chemotherapy has already commenced or been completed [+6]