Anovulation

4

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

Condition / disease
Location
Status: Not yet recruiting

Half-dose vs Conventional-dose Cetrorelix in ICSI Cycles

This prospective cohort study aims to compare the effectiveness of half-dose (0.125 mg/day) versus conventional-dose (0.25 mg/day) cetrorelix in GnRH antagonist ICSI cycles regarding clinical pregnancy rate in women with BMI ≥25 kg/m².

Participants needed: 160
Trial details
Age: 18-34Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Sep 23, 2026
Eligibility criteria

- Age less than 35 years [+3]

- Age greater than 35 years [+4]

Status: Recruiting

Sperm Preparation Prior to Intrauterine Insemination Study

This is a randomized controlled trial comparing density gradient centrifugation and microfluidic sperm sorting in patients undergoing intrauterine insemination to evaluate cumulative pregnancy outcomes.

Participants needed: 270
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Sep 15, 2026Locations: 1
Eligibility criteria

Patients undergoing intrauterine insemination [+1]

Any significant disease or psychiatric disorder that would interfere with the co... [+3]

Status: Recruiting

Letrozole Extended vs Traditional Therapy for Ovulation Induction in Women With PCOS (PROLEx-PCOS)

This randomized clinical trial aims to compare the efficacy and safety of extended letrozole therapy (5 mg/day for 10 days) versus standard letrozole therapy (5 mg/day for 5 days) for ovulation induction in women with polycystic ovary syndrome (PCOS). A total of 84 women aged 18-40 years will be randomized into two groups. Ovulation will be monitored by transvaginal ultrasound and confirmed with urinary LH testing and/or corpus luteum presence. The primary outcome is ovulation rate, while secondary outcomes include number and size of mature follicles, clinical pregnancy rate, multiple pregnancy rate, miscarriage rate, number of cycles until pregnancy, and incidence of ovarian hyperstimulation syndrome (OHSS).

Participants needed: 20
Trial details
Age: 18-40Biological sex: FemaleType: InterventionalSponsor: GABRIEL MONTEIRO PINHEIROUpdated: Nov 28, 2025Locations: 1
Eligibility criteria

Women aged 18 to 40 years; [+4]

Age <18 or >40 years; [+6]

Status: Recruiting

Effect of Vitamin D on Ovulation Rate in Women With Polycystic Ovary Syndrome

This is a randomized double-blind controlled trial on the effect of vitamin D supplementation to assess the ovulation rate of women with polycystic ovary syndrome (PCOS) and other reproductive, endocrine and metabolic outcomes after one year of treatment.

Participants needed: 220
Trial details
Age: 18-40Biological sex: FemaleType: InterventionalSponsor: The University of Hong KongUpdated: May 14, 2024Locations: 3
Eligibility criteria

Premenopausal [+4]

Use of hormonal medication (including contraception) within 3 months prior to st... [+6]