Clinical trials

158

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

Condition / disease
Location
Status: Not yet recruiting

SEPA+PrEP-Women Pilot Trial for HIV Prevention Among Women at Risk for HIV

The purpose of this study is to evaluate the preliminary efficacy of SEPA (SEPA (Salud/Health, Educación/Education, Prevención/Prevention, Autocuidado/Self-Care) +PrEP (Pre-Exposure Prophylaxis) -Women in a randomized pilot trial (N=70 women at risk for HIV; 35 intervention, 35 control). The primary outcome is PrEP uptake (attendance at a PrEP initiation appointment and/or receipt of a PrEP prescription, and intention to use PrEP), measured at baseline, 1-month post-intervention, and 3 months post-intervention. The control group will receive SEPA+PrEP-Women after the 3-month assessment (delayed intervention). We hypothesize that women assigned to SEPA+PrEP-Women will demonstrate higher PrEP uptake than controls, yielding initial effect size estimates to power a future definitive trial. Secondary outcomes include changes in sexual HIV risk behaviors, PrEP knowledge, and PrEP intentions.

Participants needed: 70
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Oct 8, 2026Locations: 1
Eligibility criteria

Self-identify as a woman [+6]

Does not meet the applicable inclusion criteria [+2]

Status: Recruiting

Auricular Vagus Nerve Stimulation Mechanisms for HIV-Associated Peripheral Neuropathy

This study looks at a non-invasive ear stimulation treatment to better understand nerve pain in people living with HIV. The study aims to assess how the body and nervous system respond to this treatment, including changes in heart function and pain signals. The goal is to learn how future treatments for nerve pain may be improved.

Participants needed: 70
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 6, 2026Locations: 1
Eligibility criteria

Established HIV infection [+4]

Unstable cardiac disease [+9]

Status: Not yet recruiting

Eye-Tracking Alcohol Warning

This pilot study will evaluate communication strategies that may improve public understanding of alcohol-related cancer risks and influence behavioral intentions. The study will compare graphic alcohol cancer warning labels with the current U.S. Surgeon General text-only warning label across two stages. The first stage is an in-person, lab-based eye-tracking experiment that will examine differences in visual attention, communication outcomes, harm perception, and behavioral intentions following exposure to graphic versus text-only warning labels. The second stage is a discrete choice experiment that will examine how warning label type, warning label size, and alcohol type (beer, wine, or liquor) influence participants' intentions to reduce or stop alcohol consumption and purchase alcohol. The study will recruit 50 adults aged 21 years or older who report regular alcohol consumption.

Participants needed: 50
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 1, 2026Locations: 1
Eligibility criteria

Age ≥ 21 years [+5]

Are not regular alcohol consumers (< 2 drinks per week) [+4]

Status: Not yet recruiting

Alternate Pre-med in Anti-Cluster of Differentiation 20 (CD20) Pilot Project

The purpose of this study is to assess and compare how well multiple sclerosis (MS) patients tolerate cetirizine versus diphenhydramine as a pre-medication before receiving anti-CD20 infusion therapy of ocrelizumab, ublituximab or rituximab. The study will also compare the safety of cetirizine versus diphenhydramine as a pre-medication for preventing infusion reactions in MS patients receiving anti-CD20 infusion therapy.

Participants needed: 60
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 2, 2026Locations: 1
Eligibility criteria

Ages ≥18 years [+4]

Adults unable or unwilling to consent [+5]

Status: Not yet recruiting

Post-op Analgesia of Nail Unit Procedures

The purpose of this study is to directly compare the efficacy of suzetrigine vs. oxycodone+acetaminophen vs. alternating acetaminophen/ibuprofen in controlling post-operative pain after the following nail unit procedures.

Participants needed: 45
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 1, 2026Locations: 1
Eligibility criteria

All patients age 18+ able to understand and provide written consent in English o...

Patients under the age of 18 or adults unable to consent. [+1]

Status: Recruiting

Florida Community-Engaged Research Alliance (FL-CEAL)

The purpose of the study is learn more about ways to help people with non-medical issues that can affect participant health. The study team will examine if Community Health Workers, members of a community who provide basic health and medical care within communities, are more helpful to people with non-medical issues than simple reading materials on how participants can do it themselves.

Participants needed: 900
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 1, 2026Locations: 7
Eligibility criteria

Individuals living within the target community who do not plan to move out of th... [+7]

Are unable or unwilling to consent [+3]

Status: Recruiting

Effects of an Exercise Program on Reaction Time and Mouse Accuracy in Recreational Video Game Players

This study is intended to evaluate the effects of an exercise program on the change of electronic sports (esports) athletes' reaction time and mouse click accuracy. The benefits of participation are directly related to exercise, and include improved thinking, performance, sleep, and quality of life.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Oct 1, 2026Locations: 1
Eligibility criteria

Minimum age is 18, and there is no maximum. [+2]

Individuals who are not able to participate in a full body exercise program, whe... [+2]

Status: Recruiting

Binaural Beats for Postoperative Pain and Anxiety Reduction

To deliver a 30-minute binaural beats audio intervention in PACU and collect pain and anxiety outcomes immediately following surgery, and 4 hours following surgery completion in adults undergoing ambulatory total knee arthroplasty and total hip arthroplasty (TKA and THA).

Participants needed: 50
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

American Society of Anesthesiologists Physical Status Classification System (ASA... [+3]

Moderate-severe hearing impairment or use of hearing aids [+3]

Status: Recruiting

Food Intake and Thermogenesis in High Spinal Cord Injury

The purpose of this research is to determine the effects of food on cardiovascular and metabolic health in men with and without spinal cord injury (SCI).

Participants needed: 56
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Men and Women [+5]

Uncompensated thyroid disease [+6]

Status: Recruiting

Geolocation Positional System (GPS) Experience

The purpose of this study is to use smartphone technology to capture individual location emotional and cognitive data, to examine how real-world behaviors thoughts, emotions, and brain activity are related to one another.

Participants needed: 100
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Must agree to give informed consent [+3]

history of head trauma, seizures, or neurological disorders [+6]

Status: Recruiting

Velocity-Loss Training and Parkinson's Disease

This study will compare the effects of velocity-loss resistance training at 10% and 30% velocity loss thresholds on measures of muscle strength and power and tests of daily performance in older adults with Parkinson's disease.

Participants needed: 60
Trial details
Age: 50-85Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

Parkinson's Disease Hoehn & Yahr Stages 1-3 [+2]

Uncontrolled cardiovascular or other neuromuscular disease that prevent particip... [+2]

Status: Recruiting

Spinal Cord Injury Model Systems (SCIMS) - Education Module

The purpose of this study is to find out if receiving education regarding increased risks of cardiometabolic disease helps subjects understand these risks and how these risks participants' health.

Participants needed: 250
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 30, 2026Locations: 3
Eligibility criteria

Men and Women with SCI/D aged 18-70 years. [+2]

Pregnancy determined by urine testing in sexually active females. [+3]

Status: Recruiting

Tailored Anti-Inflammatory American Diet for Patients With Crohn's Disease

The purpose of this study is to test the effect of an anti-inflammatory diet tailored for patients living in the United States with Crohn's Disease (CD) on clinical symptoms and disease inflammation and to identify biomarkers of response to dietary therapy.

Participants needed: 122
Trial details
Age: 16-75Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Documented diagnosis with Crohn's Disease from medical records. [+1]

Diagnosis of Ulcerative Colitis (UC). [+15]

Status: Recruiting

Pembrolizumab and Lenvatinib in Mismatch Repair Proficient Recurrent Endometrial Cancer After Progression on or Following First-Line Immunotherapy Maintenance

The purpose of this study is to determine the efficacy and safety of Pembrolizumab in combination with Lenvatinib in recurrent, mismatch repair-proficient endometrial cancer after failure of first-line therapy with a platinum-based doublet chemotherapy and immunotherapy.

Participants needed: 46
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Histologically confirmed recurrent endometrial carcinoma, including serous, endo... [+15]

Uterine sarcoma [+12]

Status: Recruiting

NSAID Use After Robotic Partial Nephrectomy

The purpose of this study is to see how effective non-steroidal anti-inflammatory drugs (NSAIDs) are at controlling pain without side effects in participants after robotic-assisted partial nephrectomy.

Participants needed: 110
Trial details
Phase: Phase 2Age: 18-99Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Patients undergoing uncomplicated robotic assisted laparoscopic partial nephrect... [+2]

Allergy to NSAIDs [+8]

Status: Recruiting

Remotely-Delivered Cognitive Behavioral Stress Management for Breast Cancer (R-CBSM)

The purpose of this research study to find out if a program called Remotely-delivered Cognitive Behavioral Stress Management (R-CBSM) can help women with breast cancer in the period of survivorship after they have completed treatment. This is a group stress management program done from home using technology, like Zoom to conduct video calls to conduct group-based training in stress management techniques (e.g., relaxation, cognitive behavioral therapy, coping skills training) in a supportive environment. It is for women aged 50 or older who have finished their main breast cancer treatments (like surgery, radiation, or chemo) and are undergoing hormone treatment. This study is important because many breast cancer survivors still feel stress, even after treatment ends. Teaching stress management may help the body and mind work better and may slow down the effects of aging caused by cancer and stress.

Participants needed: 192
Trial details
Age: 50+Biological sex: FemaleType: InterventionalSponsor: University of MiamiUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

50 yrs or older [+8]

Unable or unwilling to provide informed consent [+6]

Status: Recruiting

Implementing Depression and Adherence Treatment

The goal of this clinical trial is to compare a core set and enhanced set of implementation strategies in increasing the reach of evidence-based treatments to patients with HIV and depression. The main questions it aims to answer are: What proportion of patients start an evidence-based treatment for depression (reach)? What percentage of patients show clinical improvement in depression and what percentage attain viral undetectability within one year (effectiveness)? Researchers will compare high and low reach clinics to further inform tailored implementation strategies for uptake and maintenance. Clinics will be randomized into one of two study arms: core versus enhanced strategies. In both arms, core strategies will be utilized. Enhanced clinics will also receive more resource-intensive training.

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Clinics are eligible if they provide HIV primary care via the City of Cape Town... [+4]

Status: Recruiting

Precise Oncology Interventions in Nutrition and Training (OnPoint)

The purpose of this study is to see if survivors of breast, prostate, colorectal or lymphoma cancer who receive a personal referral to a targeted nutrition and exercise program will be able to eat a healthier diet and be more physically activity.

Participants needed: 306
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Provide full- or part-time care in an oncology clinical care setting at Sylveste... [+11]

Less than 18 years of age [+11]

Status: Recruiting

Combating Alzheimer's Through Sleep and Exercise

The Combating Alzheimer's through Sleep and Exercise (CASE) study is an exploratory, hypothesis-generating trial designed to: (1) assess whether improvements in sleep are associated with improvements in cognitive performance and cardiovascular and metabolic health; (2) evaluate the effects of structured, moderate-level aerobic and anaerobic exercise on cognitive performance and cardiovascular and metabolic health; (3) examine the combined, potentially synergistic effects of both interventions on cognitive performance and cardiovascular and metabolic health; and (4) investigate the role of light exposure as a potential modulator of sleep parameters.

Participants needed: 60
Trial details
Age: 55-80Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Aged 55-80 years at the time of the screening visit [+9]

Severe mobility limitations that prevent safe participation in moderate exercise... [+9]

Status: Not yet recruiting

Exercise-induced Steroid Changes in Active Surveillance for Prostate Cancer

The purpose of this research study is to understand how a short session of a home-based bodyweight high-intensity interval training (HIIT) affects steroid hormone levels in men on active surveillance for low-grade prostate cancer.

Participants needed: 49
Trial details
Age: 18-80Biological sex: MaleType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Males 18 to 80 years old [+6]

Males currently receiving treatment for prostate cancer [+5]

Status: Recruiting

Utility of ctDNA in Early Switch of First-line Chemotherapy in Metastatic Pancreatic Ductal Adenocarcinoma

The purpose of this study is to understand whether a blood-based test called circulating tumor DNA (ctDNA) can detect whether participants are having a desired tumor shrinkage or an undesired lack of tumor shrinkage, and to study whether these levels of ctDNA can be used to make treatment decisions faster than the current standard approach, which is to wait 8 weeks after starting chemotherapy to obtain participant first imaging scans since starting chemotherapy.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Histologically confirmed, metastatic pancreatic adenocarcinoma. Patients with ad... [+16]

Patients with pure neuroendocrine neoplasms of the pancreas. [+15]

Status: Recruiting

Open-label of Loncastuximab Tesirine (ADCT-402) in Relapsed/Refractory Marginal Zone Lymphoma

The purpose of this research study is to see if loncastuximab tesirine has any benefits at dose levels researchers found acceptable in earlier studies in patients with related forms of immune cell cancers. The researchers want to find out the effects (good and bad) that loncastuximab tesirine has on the participant and the participant's condition.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 4
Eligibility criteria

Men and women, aged 18 years or older. [+30]

Evidence of DLBCL transformation. a. Subjects with presumptive evidence of trans... [+22]

Status: Recruiting

ERd Combination Treatment in Newly Diagnosed Multiple Myeloma (ADVANCE 2.0)

The purpose of this study is to determine the effects that Elranatamab in combination with Lenalidomide and Dexamethasone has on participants that have been newly diagnosed with Multiple Myeloma.

Participants needed: 104
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Serum monoclonal protein ≥ 1.0 g/dL [+17]

Adult male and female participants ≥ 18 years of age. [+52]

Status: Recruiting

Unified Protocol: Community Connections

The purpose of this study is to administer the Unified Protocols for Transdiagnostic Treatment of Emotional Disorders in Children (UP-C) and Adolescents (UP-A) to youth and participants' parents and to examine the efficacy and outcomes of the treatment using standardized measures, questionnaires, interviews. The UP-C and the UP-A are cognitive-behavioral therapies to treat emotional disorders.

Participants needed: 1,500
Trial details
Age: 7-17Biological sex: AllType: InterventionalSponsor: University of MiamiUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Children between the ages of 7-17. [+6]

Prior receipt of at least 8 sessions of the UP-C/A program at the Child and Adol... [+3]

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: Sep 16, 2026Locations: 1
Eligibility criteria

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

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