Clinical trials

156

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Active Versus Passive Sitting, Cognition and Energy

The study will compare cognitive capacity, muscle utilization patterns, soft tissue seated pressure and caloric output during four seated conditions: 1. passive sitting in a regular chair; 2. passive sitting in an exercise chair; 3. sitting in the exercise chair during active dynamic exercise; and, 4. sitting in the chair during active static exercise.

Participants needed: 35
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 20, 2026Locations: 1
Eligibility criteria

Adult (18-70)

Any current injury in the lower limb or trunk. [+3]

Status: Recruiting

Prophylactic Antibiotics for Outpatient Urethral Bulking

The purpose of this study is to evaluate whether taking prophylactic (preventative) antibiotics at the time of standard of care clinic-based urethral bulking reduces the risk of post-procedural urinary tract infection (UTI).

Participants needed: 150
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Aug 20, 2026Locations: 2
Eligibility criteria

Women ≥ 18 years of age. [+5]

Contraindications to both oral antibiotics including antibiotic allergies or sig... [+7]

Status: Not yet recruiting

PrEP & Soccer: A Program for Pharmacy Chains to Increase PrEP Awareness and Access Among Men

This type 3 Hybrid Effectiveness-Implementation study will evaluate PrEP \& Soccer, a multicomponent and multilevel implementation strategy delivered by a pharmacy chain to increase PrEP knowledge and initial PrEP appointment attendance among men. Using mixed methods and implementation science approaches, this parallel cluster randomized controlled study will assess key implementation factors at CVS Health pharmacy locations assigned either to the PrEP \& Soccer intervention or to a general CVS Health service information-only control.

Participants needed: 800
Trial details
Age: 18-54Biological sex: MaleType: InterventionalSponsor: University of MiamiUpdated: Aug 19, 2026Locations: 1
Eligibility criteria

Provide their informed consent to participate. [+9]

Inability to provide informed consent (e.g., cognitive impairment), or [+11]

Status: Recruiting

Preoperative Comprehensive Geriatric Assessment (CGA) and Postoperative Delirium

The purpose of this research is to find out the best way to reduce delirium in frail, older patients undergoing planned surgery. Delirium is a state of confusion and difficulty concentrating that is temporary. Delirium may make the person anxious, angry, sleepy, not think clearly, or hallucinate. Being frail in medicine means that the body may not easily recover from a stressor, such as surgery. This study will determine if a detailed on-going evaluation by a Geriatrician, doctor who specializes in the care of older adults, after surgery is better at decreasing the risk of delirium than simply highlighting the patient's frailty in the electronic medical record.

Participants needed: 200
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Frailty as measured by the 5-modified frailty index (5-mFI) during the anesthesi... [+3]

Absence or withdrawal of informed consent, [+2]

Status: Recruiting

Mental Health in Primary Care

The goal of this study is to evaluate in an effectiveness-implementation type I hybrid trial, an enhanced version of eHealth Familias Unidas for reducing depressive, anxious symptoms and suicide behavior in Hispanic youth. The study will use a randomized rollout design with 18 pediatric primary care clinics in the South Florida area.

Participants needed: 468
Trial details
Age: 12-16Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 18, 2026Locations: 17
Eligibility criteria

Female and male adolescents, who self-identify as Hispanic (or Latino(a)) [+4]

Families reporting plans to move out of the South Florida area during the study...

Status: Recruiting

Adaptive Self-Efficacy-Based AI Coaching for Cycling

The primary objective of this study is to evaluate whether adaptive, AI-delivered personalized self-efficacy-based AI coaching based on real-time physiological and performance feedback enhance indoor cycling power output during a 20-minute time trial compared to static affirmations and exercise-only control conditions.

Participants needed: 120
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 17, 2026Locations: 1
Eligibility criteria

Age 18-40 years [+3]

Cardiovascular, metabolic, or respiratory conditions [+4]

Status: Recruiting

Haptics in Virtual Reality

The purpose of this study is to investigate the role of non-invasive wearable haptic feedback, in supporting literacy-focused Virtual Reality (VR) learning environments. The haptic feedback will be delivered through haptic gloves with integrated vibration monitors and finger tracking. The primary objective is to examine how multisensory engagement, specifically the addition of haptic cues, influences learning outcomes such as phonetic recognition, spelling, and reading skills in early learners.

Participants needed: 60
Trial details
Age: 6+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 17, 2026Locations: 2
Eligibility criteria

Students from elementary to higher education; [+1]

Students with significant uncorrected vision; [+4]

Status: Recruiting

Relationship Enhancement Digital Game

The purpose of this study is to test a new digital game. Specifically, this study will aim to evaluate a digital game prototype designed to facilitate playful interactions between parents and children. The prototype will incorporate activities grounded in relationship enhancement principles. Additionally, this study will check how well using digital tools helps build strong connections, makes people get along better, and boosts parents' confidence and parenting skills.

Participants needed: 30
Trial details
Age: 6+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 17, 2026Locations: 2
Eligibility criteria

Caregiver-child dyads.

Participant is not part of a caregiver- child dyad.

Status: Recruiting

reSET for the Treatment of Stimulant Use in HIV Clinics: Care Optimization Supporting Treatment Adherence (COSTA)

The purpose of this study is to find out if reSET, an FDA authorized mobile therapeutic, is effective in treating stimulant use disorder and helping keep HIV viral load suppression stable among men who have sex with men who are living with HIV and have a stimulant use disorder.

Participants needed: 260
Trial details
Age: 18-90Biological sex: MaleType: InterventionalSponsor: University of MiamiUpdated: Aug 17, 2026Locations: 1
Eligibility criteria

Assigned male sex at birth and has not undergone any transgender hormonal treatm... [+13]

Patient appears to have diminished capacity to consent either because of cogniti... [+3]

Status: Recruiting

FAMILY Sleep Program

The purpose of this study is to learn about sleep behaviors and test different ways to help patients with cancer and partners. Participants (patient-sleep-partner caregivers dyads as a unit) participate in the study together.

Participants needed: 18
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

The eligibility criteria for patients are [+12]

having had a diagnosis of major depressive disorder, psychosis, or bipolar disor... [+6]

Status: Recruiting

Brain-Controlled Spinal Stimulation Walking Therapy After Incomplete Spinal Cord Injury (SCI)

The purpose of this research is to test the effectiveness of a new therapy, called Brain-Computer Interface (BCI)-Transcutaneous Spinal Cord Stimulation (TSCS), for improving walking in people with an incomplete spinal cord injury (SCI).

Participants needed: 12
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

At least 18 years old and no older than 70 years old at the time of enrollment. [+4]

Has traumatic brain injury, stroke, multiple sclerosis, or other neuromuscular d... [+14]

Status: Recruiting

Understanding and Treating Traumatic Brain Injury (TBI) Associated Photophobia With Botulinum Toxin Type A (BoNT-A)

The purpose of this research is to understand and treat Traumatic Brain Injury (TBI) associated photophobia (light sensitivity) and its impact on visual function.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Recruit and enroll male and female subjects, civilians and veterans (1:1 mix ant... [+5]

Individuals with ocular diseases that may confound photophobia, such as glaucoma... [+3]

Status: Recruiting

Male Fertility Program

Following spinal cord injury, most men are infertile and require medical assistance to father children. The conditions that contribute to their infertility are erectile dysfunction, ejaculatory dysfunction, and semen abnormalities. The Miami Project Male Fertility Program is a research study designed to understand and improve impairments to male fertility resulting from spinal cord injury.

Participants needed: 100
Trial details
Age: 18-50Biological sex: MaleType: ObservationalSponsor: University of MiamiUpdated: Aug 17, 2026Locations: 1
Eligibility criteria

Any man with spinal cord injury over the age of 18. Control Subjects will be any...

Women will be excluded.

Status: Recruiting

eHealth Mindfulness-based Music Therapy Intervention for Patients Undergoing Stem Cell Transplantation

The goal of this study is to test an electronic health (eHealth) mindfulness-based music therapy intervention to improve health-related quality of life and reduce symptom burden and disease activity in patients undergoing stem cell transplantation.

Participants needed: 165
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 13, 2026Locations: 1
Eligibility criteria

≥ 18 years of age [+3]

history of severe psychiatric illness (e.g., psychosis, active suicidality, inpa... [+5]

Status: Not yet recruiting

Dose Dependent Steroid Injections

This study aims to evaluate the efficacy of interlaminar steroid injections at treating pain in lumbar radiculopathy at varying doses, to evaluate the efficacy of interlaminar steroid injections at improving quality of life and function in lumbar radiculopathy at varying doses, and to evaluate difference in efficacy between triamcinolone and dexamethasone interlaminar steroid injections at treating pain in lumbar radiculopathy at varying doses, with the overarching hypotheses that there is no difference in reported pain reduction, quality of life, or function among patients receiving low, moderate, or high doses, and no difference in reported pain reduction between triamcinolone and dexamethasone.

Participants needed: 150
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Adults able to consent [+4]

Adults unable to consent [+4]

Status: Recruiting

Study Evaluating Safety, Tolerability, and Metabolism of Niraparib

The purpose of this study is to identify the genetic characteristic(s), specifically degree of African ancestry, and environmental characteristic(s) that appear to be related to the effects, both good and bad, that the maintenance treatment has women with ovarian cancer. In this study, an investigational medication called niraparib is being tested for the treatment of ovarian cancer. Niraparib works by blocking the ability of cancer cells to fix their genes. Cancer cells with damaged genes have a harder time growing and spreading in the body and can even die.

Participants needed: 70
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Aug 5, 2026Locations: 4
Eligibility criteria

Participant must be female ≥18 years of age, able to understand study procedures... [+23]

Any of the following histologies: low-grade serous carcinoma, grade 1 or 2 endom... [+18]

Status: Not yet recruiting

Miami "RADAR" Trial

The purpose of this study is to see if treating cancer with radiation therapy administered by the Varian Ethos system can control patient's tumor and eliminate the need for surgery used to treat nerves in the spine flattened by pressure (compressed).

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 4, 2026Locations: 1
Eligibility criteria

Male and female participants ages ≥ 18. [+18]

Unknown primary histology. [+8]

Status: Recruiting

SABER Study for Selected Early Stage Breast Cancer

The purpose of this study is to find the most effective dose of radiation therapy to give to breast tumors in a shorter period of time, prior to standard partial mastectomy/axillary surgery.

Participants needed: 18
Trial details
Age: 50+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Aug 3, 2026Locations: 1
Eligibility criteria

Female, ≥ 50 years of age. [+9]

Patients without histologically confirmed invasive breast cancer. [+9]

Status: Not yet recruiting

Artificially Intelligent Robot Control

The purpose of the study is to compare the impact of standard asthma education with the standard + Artificially Intelligent Robot (AIR) Control intervention.

Participants needed: 80
Trial details
Age: 4+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 3, 2026Locations: 1
Eligibility criteria

The participant must be at least 18 years old. [+7]

The participant is younger than 18 years old. [+7]

Status: Not yet recruiting

High-Intensity Functional Training (HIFT) vs Moderate-Intensity Continuous Training (MICT) in College Students

The purpose of this study is to compare two types of exercise programs in college students: high-intensity functional training and moderate-intensity continuous training. The study evaluates whether these exercise programs improve body composition, physical fitness, and blood vessel health compared with a group that does not participate in exercise training. In addition, the study examines whether changes in body composition and physical fitness are associated with changes in blood vessel health.

Participants needed: 90
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Aug 4, 2026Locations: 1
Eligibility criteria

Age 18 to 35 years. [+4]

Known cardiovascular, metabolic, pulmonary, renal, neurological, musculoskeletal... [+7]

Status: Recruiting

Spectroscopic MRI, Proton Therapy, and Avastin for Recurrent Glioblastoma

The purpose of this research is to find hidden cancer with an experimental magnetic resonance imaging (MRI) scan called spectroscopic magnetic resonance imaging (sMRI). That spectroscopic MRI scan will be used to increase the area of the brain receiving radiation and then the dose of radiation in attempt to kill more of the cancer. Proton radiotherapy and bevacizumab (Avastin) are used to minimize the possible side effects of this approach.

Participants needed: 96
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Jul 29, 2026Locations: 1
Eligibility criteria

An area of MRI enhancement consistent with glioblastoma outside of the initial h... [+10]

Unstable angina and/or congestive heart failure requiring hospitalization within... [+7]

Status: Recruiting

Guardant Shield Colorectal Cancer Screening

The purpose of this research is to identify individuals overdue for colon cancer screening and send them a reminder to complete their screening, which includes standard of care colonoscopy or stool-based testing. The investigators are randomizing patients (like a flip of a coin) to either receive the standard reminder by mail/email or to receive the standard reminder and have the option to provide a blood sample for screening (ShieldTM by Guardant).

Participants needed: 500
Trial details
Age: 45-85Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Jul 27, 2026Locations: 1
Eligibility criteria

Adults 45 - 85 years of age at average risk and able to provide informed consent... [+1]

Impaired decision-making capability/unable to provide informed consent. [+6]

Status: Recruiting

Autologous Serum Tears With Hyaluronate vs Balanced Salt Solution for Moderate-to-Severe Dry Eye

This study aims to find out whether adding sodium hyaluronate, a moisturizing ingredient commonly found in artificial tears, makes autologous serum eye drops more effective for treating moderate-to-severe dry eye disease. Each participant will use one version of the drops in one eye and the standard version in the other eye. The goal is to see if the new combination provides better relief, comfort, and eye surface healing compared to the traditional formulation.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years old [+5]

Age <18 years old. [+4]

Status: Recruiting

Facial Papules in Frontal Fibrosing Alopecia (FFA)

The objective is to evaluate the safety and efficacy of the Cutera 1726 nm laser system (also referred to as AviClear) for the treatment of facial papules in frontal fibrosing alopecia (FFA).

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

Female or Male [+9]

Prior treatment to the target area during participation in a clinical trial of a... [+16]

Status: Recruiting

Rosacea Radiofrequency Microneedling

There are 3 main objectives of this proposal as follows: (1) to assess the efficacy of radiofrequency microneedling in the treatment of erythematotelangiectatic and or papulopustular rosacea, (2) to determine the potential for combination treatment of radiofrequency microneedling with the 532 nm KTP laser, and (3) identify potential novel therapeutic strategies for the treatment of rosacea.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Jul 24, 2026Locations: 1
Eligibility criteria

Male or female adult (>18yo) subjects in general good health [+3]

Patients currently utilizing oxymetazoline or brimonidine. [+7]