Polycystic Ovary Syndrome

48

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

Condition / disease
Location
Status: Recruiting

The Physiological Responses and Adaptation of Brown Adipose Tissue to Chronic Treatment With Beta3-Adrenergic Receptor Agonists

Background: Brown adipose tissue (BAT) is a type of fat in the body. It may prevent weight gain, improve insulin sensitivity, and reduce fatty liver. Researchers want to see if BAT helps the body burn energy. Objective: To learn more about how BAT works to burn energy. Eligibility: People ages 18-40 with a body mass index between 18 and 40 Design: Participants will be screened with: Medical history Physical exam Blood, urine, and heart tests Dietitian interview Participants will have an overnight baseline visit. This includes: Repeats of screening tests Exercise test Scans. For one scan, a radioactive substance is injected into the arm. FSIVGIT: An IV is inserted into veins in the right and left arms. Glucose and insulin are injected in one arm. Blood glucose and insulin levels are measured from the other. Metabolic suite: Participants stay 18-19 hours in a room that measures their metabolic rate. Monitors on the body measure heart rate, movement, and temperature. Optional fat biopsy: A small piece of tissue is removed with a needle. Participants will take 2-4 pills daily for 4 weeks. All women will take the drug mirabegron. Men will be randomly get either the drug or a placebo. All participants will have a visit after 2 weeks of the pills. They will repeat the screening tests. Participants will have an overnight visit 2 weeks later. They will repeat the baseline tests. Participants will keep food and medication diaries. Participants will have a follow-up visit 2 weeks after stopping the pills. This includes heart tests.

Participants needed: 100
Trial details
Phase: Phase 1Age: 18-40Biological sex: AllType: InterventionalSponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Updated: Jun 1, 2026Locations: 1
Eligibility criteria

Female [+17]

Hypersensitivity and associated allergic reactions to mirabegron (or similar dru... [+28]

Status: Not yet recruiting

Observational Study on the Causal Architecture of Polycystic Ovary Syndrome (PCOS)

The goal of this observational study is to learn about the causal architecture of Polycystic Ovary Syndrome (PCOS) in women aged 18 to 45. The main questions it aims to answer are: What does the hormonal, metabolic, and clinical architecture of PCOS look like across a diverse global population? Can the causal architecture of PCOS be reconstructed from existing lab results and clinical data? Are there distinct architectural patterns across different groups of women with PCOS? Participants who have been diagnosed with PCOS by a healthcare provider will complete an online questionnaire about their diagnosis, symptoms, clinical history, current treatment, and existing lab results. Participants will also be asked to submit copies of their most recent blood work and lab results. No intervention or treatment is involved. All data is de-identified.

Participants needed: 100
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: AnnieGuard Corp.Updated: Jun 3, 2026
Eligibility criteria

Female [+4]

Under 18 years of age [+3]

Status: Recruiting

Combined Oral Contraceptive Pill and Resistance Starch

This study will enroll women with PCOS to study the effects of first line therapy, oral contraceptive pills, and then either 12 weeks of resistant starch or 12 weeks of placebo to explore if resistant starch improves cardiometabolic parameters or impacts gut dysbiosis compared to placebo.

Participants needed: 100
Trial details
Phase: Phase 2Age: 18-40Biological sex: FemaleType: InterventionalSponsor: University of PennsylvaniaUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Women between ages of 18-40 years with BMI greater than or equal to 25 kg/m² to... [+3]

Subjects with other causes for irregular menses such as pregnancy, lactation, un... [+17]

Status: Recruiting

Determinants of Insulin Sensitivity by Age, Sex, Race/Ethnicity, BMI, and PCOS Diagnosis

The study aims to investigate the relationship between fasting insulin and Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) across various demographic factors, including age, sex, race/ethnicity, BMI, and polycystic ovary syndrome (PCOS) diagnosis. By analyzing these variables, the study seeks to identify potential variations in insulin levels, which could provide valuable insights into the impact of different factors on metabolic health and the development of insulin-related conditions.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ali ChappellUpdated: May 1, 2026Locations: 1Duration: 1 Year
Eligibility criteria

Fasting insulin [+3]

Status: Recruiting

Interest of Myo-inositol Supplementation in Women With Polycystic Ovarian Syndrome

The main objective will be to check if MyoInositol (MYO) reduces the total resistance rate to Clomiphene Citrate (CC). For this, our study will be controlled, randomized and double blinded. It will include patients with PCOS (polycystic ovary syndrome, defined by the Rotterdam criteria) who wish to become pregnant and are eligible to simple ovulation induction by CC. Half of them will receive MYO + levomefolic acid (5-MTHF) in addition to the CC, while the other half will receive a placebo containing only 5-MTHF in addition to the CC. The MYO supplementation will be initiated at least one month before taking CC and will be continued throughout this treatment until pregnancy or before switching to another type of treatment for ovulation induction if no pregnancy is obtained after 6 ovulatory cycles.

Participants needed: 276
Trial details
Phase: Phase 3Age: 18-35Biological sex: FemaleType: InterventionalSponsor: University Hospital, LilleUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Wishing pregnancy, [+4]

Intolerance to CC in previous treatment, [+6]

Status: Recruiting

Glucose Profiles in Women With Polycystic Ovary Syndrome

Polycystic ovary syndrome is a very common condition that is associated with metabolic complications. Patients with polycystic ovary syndrome exhibit insulin resistance and are at greater risk to develop type 2 diabetes. This syndrome is heterogeneous, classified according to 4 phenotypes (A-D). It seems that certain phenotypes are less exposed to insulin resistance and metabolic complications. However, only a few studies have evaluated the glucose profile according to phenotype. New technologies now make it possible to monitor glucose levels continuously. The aim of this project is to evaluate glucose profile parameters using continuous glucose monitoring, and to compare these profiles according to different PCOS phenotypes.

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Centre Hospitalier Universitaire, AmiensUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Age > 18 years at inclusion criteria [+3]

Pregnancy, breast-feeding [+3]

Status: Not yet recruiting

Berberine Phytosome for Signs and Symptoms of Polycystic Ovary Syndrome (PCOS)

This multicenter, randomized, controlled clinical trial aims to evaluate the effectiveness of berberine phytosome supplementation in improving signs and symptoms associated with polycystic ovary syndrome (PCOS). Women presenting with clinical features suggestive of PCOS, including hirsutism, acne, menstrual irregularities, and overweight, will be enrolled. Participants will be randomly assigned to one of three groups: (1) berberine phytosome supplementation in women not previously taking inositol, (2) berberine phytosome supplementation in women already taking inositol for at least three months, or (3) a control group receiving lifestyle advice without supplementation. The intervention will consist of berberine phytosome 550 mg once daily for 12 weeks. The study will evaluate changes in clinical manifestations associated with hyperandrogenism and metabolic dysfunction, including hirsutism, acne severity, body mass index, and metabolic parameters. The results will provide evidence on the potential role of berberine phytosome supplementation in improving clinical manifestations related to PCOS.

Participants needed: 150
Trial details
Age: 18-40Biological sex: FemaleType: InterventionalSponsor: Liaquat University of Medical & Health SciencesUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Women aged 18-40 years [+5]

Pregnancy or breastfeeding [+6]

Status: Recruiting

Study of the Effect of a Nutritional Supplement on Microbiota, Metabolic Control, Inflammatory Profile, and Quality of Life in Patients With Polycystic Ovary Syndrome.

Polycystic Ovary Syndrome (PCOS) is a complex endocrine-metabolic disorder characterized by elevated androgen levels due to ovarian overproduction. Although the pathophysiology of PCOS is not fully understood, it is estimated that insulin resistance (IR) occurs in 70-80% of PCOS cases, which may contribute to hyperandrogenism in affected women. Women with PCOS and IR are more likely to develop metabolic syndrome, increasing the risk of diabetes, cardiovascular diseases, lipid profile deterioration, elevated inflammation levels, and greater oxidative stress. The symptoms of PCOS are varied and differ among patients. Common symptoms include androgenic alopecia, hirsutism, acne, abdominal fat accumulation, and fertility issues. These physical manifestations and related problems have been associated with reduced quality of life and self-esteem in these women. The symptoms of PCOS can be improved through lifestyle changes aimed at enhancing insulin sensitivity, such as proper nutrition and regular physical exercise. Some supplements, such as a combination of Myo-inositol and D-chiro-inositol in a 40:1 ratio, are being used to support the management of PCOS because they appear to improve insulin sensitivity, as well as reduce underlying inflammation and oxidative stress. To determine whether nutritional intervention combined with inositol supplementation improves PCOS symptoms, various variables will be analyzed to assess improvements in oxidative stress markers, inflammation, lipid profile, hormonal profile, and microbiota. Additionally, if the metabolic profile improves, it is hypothesized that this could also enhance quality of life and self-esteem.

Participants needed: 120
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Celia BañulsUpdated: Mar 17, 2026Locations: 1
Eligibility criteria

Patients aged between 18 and 45 years. [+2]

Having been treated with medication or supplementation aimed at improving PCOS p... [+7]

Status: Recruiting

Multidisciplinary Diagnosis and Treatment of Polycystic Ovary Syndrome

The investigators collected clinical data and serum samples of patients with polycystic ovary syndrome (PCOS) in this study, used statistical software such as SPSS for date analysis, and used experimental techniques such as ELISA and flow cytometry to detect serum samples, aiming to explore the relationship between the body anthropometry, skin conditions, psychosomatic status, diet, sleep, exercise, glucose and lipid metabolism, gonadal hormones, and body fat distribution in patients with polycystic ovary syndrome, and to discovery new biomarkers. Multidisciplinary exploration of the mechanisms of disease occurrence and development, the establishment of a PCOS multicenter, multidisciplinary and multidimensional clinical research database, combined with the established statistical analysis strategy for big data and analysis, to promote the realization of more accurate personalized medicine.

Participants needed: 3,000
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Shanghai 10th People's HospitalUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Female aged 18- 45;

Female patients younger than 18 years old or older than 45 years old; [+10]

Status: Recruiting

Is There a Benefit From Addition of Physical Exercise to Diet Restriction/Limitation in PCOS Women With Asthma?

Women with polysyctic ovarian syndrome (PCOS) usually develop many complications including asthma. Nowdays, diet restriction combimed with phsyical exercises may improve both problems

Participants needed: 40
Trial details
Age: 20-30Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Mar 3, 2026Locations: 1
Eligibility criteria

PCOS women [+2]

cardiac problems [+2]

Status: Not yet recruiting

Identification of Women With Severe Insulin Resistant Syndromes of Genetic Origin Among Patients With "Classic" Polycystic Ovary Syndrome (PCOS)

Diagnostic case-control study (1 case for 2 controls). Inclusion of patients with severe insulin resistance syndrome of genetic origin, then inclusion of controls: patients examined for PCOS in day hospital with matching age (+/- 5 years) and Body mass index (+/- 5kg/m2).

Participants needed: 81
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Women aged ≥ 18 years and < 45 years ; [+3]

- Severe renal insufficiency (GFR < 30 ml/min) ; [+8]

Status: Recruiting

The Effect of Therapy Combination in PCOS With Dlbs 3233

The effect of combination therapy dlbs 3233 and clomifen citrate vs clomifen citrate on homa ir, maturation follicle, and menstrual cycle in PCOS cases at Muhammadiyah Asri Medical Center Hospital

Participants needed: 90
Trial details
Phase: Early Phase 1Age: Up to 45Biological sex: FemaleType: InterventionalSponsor: InlacinpenelitianUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

married agree to join this research

dis agree to join research

Status: Recruiting

PCOS and Problem of Eye Dryness: Is There a Benefit From Lifetyle Changes

Women with polycystic ovarian syndrome (PCOS) may complain dryness of their eyes especially obese ones. lifestye changes are main treatrment fro both problems

Participants needed: 40
Trial details
Age: 30-40Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

PCOS women [+2]

liver disoease [+2]

Status: Not yet recruiting

Light Fasting Diet and Magnesium in Polycystic Ovary Syndrome (PCOS)

Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women of reproductive age, which is associated with hormonal imbalances, dyslipidemia, chronic inflammation, and increased oxidative stress, and can increase the risk of cardiovascular and metabolic diseases. Evidence suggests that nutritional interventions play an important role in improving metabolic outcomes in these patients. This study is a randomized, triple-blind, controlled clinical trial designed to investigate the effect of a light fasting diet combined with magnesium supplementation on lipid profile, lipid peroxidation (malondialdehyde), and C-reactive protein (CRP) levels in women with PCOS. In this study, 46 eligible women were randomly divided into two groups receiving a light fasting diet with magnesium supplementation or placebo, and changes in biochemical and anthropometric indices were evaluated before and after 8 weeks of intervention.

Participants needed: 46
Trial details
Age: 19-65Biological sex: FemaleType: InterventionalSponsor: Behnood AbbasiUpdated: Jan 7, 2026
Eligibility criteria

People between the ages of 19 and 65 [+2]

Failure of the participant to cooperate during the study [+6]

Status: Recruiting

Is There a Benefit From Addition of Treadmill Walking to Diet Restriction in Psoriasis Women With PCOS?

Women with psoriasis usually develop many complications including polysyctic ovarian syndrome (PCOS). Nowdays, diet restriction combimed with phsyical exercises may improve both problems

Participants needed: 40
Trial details
Age: 35-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

obese (class I) women [+2]

cardiac dysfucntions [+3]

Status: Recruiting

Weight Cycling on Hyperandrogenemia and Insulin Resistance in Polycystic Ovary Syndrome

This study prospectively includes PCOS patients with normal weight and overweight/obesity, closely follows up and intensively manages them, and observes the level and distribution of weight reduction achieved by patients after lifestyle intervention (high-protein diet for weight loss). Additionally, it aims to provide reference for setting weight loss targets for future PCOS patients by comparing the differences in clinical improvement among patients achieving different degrees of weight reduction (\<2% \[equivalent to no weight loss\], 2-5%, 5-10%, ≥10%) at different time points (3 months, 6 months) following dietary intervention. Furthermore, this study will compare the differences in reproductive and metabolic marker improvements between baseline PCOS patients experiencing weight rebound, those who successfully lost weight, and those who experienced weight rebound. This will help explore the impact of weight cycling on PCOS-related manifestations. Finally, at a genetic level, the study will analyze potential mechanisms underlying different outcome indicators by comparing differences in metagenomics, transcriptomics, and metabolomics among patient groups. Ancillary/Nested Sub-study (12-week Precision Nutrition Trial): Within the WHIP cohort, we will conduct a nested, prospective interventional sub-study to evaluate the efficacy of an insulin-resistance-phenotype-guided precision dietary prescription versus a standard guideline-based energy-restricted diet. Eligible participants are women with PCOS and insulin resistance enrolled in the cohort. The sub-study lasts 12 weeks with assessments at baseline and week 12. Primary endpoints include change in HOMA-IR and change in the core11 metabolic risk composite. Secondary endpoints include changes in gonadotropins (FSH, LH), sex steroid hormones (e.g., estradiol, progesterone), and patient-reported symptom scores.

Participants needed: 425
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Dec 3, 2025Locations: 1
Eligibility criteria

Women aged 18-45 years in the reproductive period; [+3]

Currently pregnant or lactating, or have had a recent (within 6 months) plan for... [+7]

Status: Recruiting

Body Fat as Determinant of Female Gonadal Dysfunction

Reproduction requires from women enough energy depots to warrant an adequate nutritional supply to the fetus. Hence, adipose tissue is able to communicate with female hypothalamic-pituitary-ovary axis. The hypothesis of the project is that abnormalities in the quantity (absolute and relative to lean body mass), distribution and/or function of adipose tissue are associated with functional forms of female gonadal dysfunction in predisposed women, in a spectrum of anomalies that go from hypothalamic amenorrhea to the polycystic ovary syndrome (PCOS). To challenge this hypothesis, the investigators will study 5 groups of 10 women each: women with exercise-associated hypothalamic amenorrhea, women without ovulatory dysfunction that exercise equally, non-hyperandrogenic patients with PCOS, hyperandrogenic patients with PCOS, and healthy control women comparable to those with PCOS. The aims of the study will be: Primary objective: To identify novel signalling factors originating from adipose tissue and muscle using targeted and nontargeted evaluation of the proteome and of gene expression of superficial subcutaneous fat, deep subcutaneous fat (which mimics visceral adipose tissue) and skeletal muscle. Secondary objectives: 1. To study the serum adipokine profile - including those identified by the primary objective - and circulating gut hormones during fasting and after a glucose load in the 5 groups of women, and their associations with sexual hormones and body fat distribution. 2. To study body composition and body fat distribution in these women and their relationships with: 2.1, Sex steroid profiles. 2.2. Classic cardiovascular risk factors: carbohydrate metabolism, lipid profiles and blood pressure. 2.3 Markers of low-grade chronic inflammation. 2.4. Oxidative stress markers. 2.5. Cardiovascular autonomic function. 2.6. Surrogate markers of subclinical atherosclerosis. 2.7. Circulating concentrations of endocrine disruptors. 2.8. Oral and gut microbiome. The results will provide a better understanding of the mechanisms linking body energy depots with the female reproductive axis and, hopefully, the identification of potential biomarkers for the diagnosis and treatment of the disorders studied here.

Participants needed: 50
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y CajalUpdated: Aug 12, 2025Locations: 1
Eligibility criteria

Body mass index between 18.5 and 25.0 kg/m2. [+21]

Oral drugs interfering with ovulation (glucocorticoids, antipsychotics, antidepr... [+4]

Status: Recruiting

PEPPI Study: Identification of Women at Risk for Placental Dysfunction

The main purpose of this study is to evaluate Fetal Medicine Foundation's pre-eclampsia risk calculator using maternal characteristics, first trimester serum placental growth factor (PlGF) and mean arterial pressure (MAP) in a Finnish general population. Condition or disease: pre-eclampsia, intrauterine growth restriction, polycystic ovary syndrome

Participants needed: 3,000
Trial details
Biological sex: AllType: ObservationalSponsor: Oulu University HospitalUpdated: Aug 5, 2025Locations: 1Duration: 15 Years
Eligibility criteria

Pregnant (first trimester) [+3]

Multiple pregnancy [+18]

Status: Recruiting

Does Spironolactone Normalize Sleep-wake Luteinizing Hormone Pulse Frequency in Pubertal Girls With Hyperandrogenism?

The purpose of this study is to determine if, in mid- to late pubertal girls with hyperandrogenism (HA), androgen-receptor blockade (spironolactone) alone normalizes sleep-wake luteinizing hormone (LH) pulse frequency (primary endpoint) and overall LH and follicle-stimulating hormone secretion (secondary endpoints).

Participants needed: 32
Trial details
Phase: Early Phase 1Age: 10-17Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Mid- to late pubertal adolescent girls as signified by either (a) post-menarchea... [+3]

Inability/incapacity to provide informed consent [+25]

Status: Recruiting

Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome

The purpose of this study is to determine if estradiol augmentation of luteinizing hormone (LH) secretion secretion (primary endpoint) and follicle-stimulating hormone (FSH) secretion (secondary endpoint) is reduced in adult women with polycystic ovary syndrome.

Participants needed: 37
Trial details
Phase: Early Phase 1Age: 18-30Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

PCOS group: post-pubertal (> 4 years post-menarche) adult woman aged 18-30 years... [+4]

Inability/incapacity to provide informed consent [+25]

Status: Recruiting

Hyperandrogenemia and Altered Day-night LH Pulse Patterns

The purpose of this study is to determine if, in mid- to late pubertal girls with hyperandrogenism, androgen-receptor blockade (spironolactone) improves the ability of progesterone to acutely reduce waking luteinizing hormone pulse frequency (primary endpoint).

Participants needed: 32
Trial details
Phase: Early Phase 1Age: 10-17Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Mid- to late pubertal adolescent girl (at least Tanner breast stage 3, but no mo... [+4]

Inability/incapacity to provide informed consent [+24]

Status: Recruiting

Lifestyle Medicine: Establishing Clinical Approaches to Chronic Disease for Rural Patients

Developed nations worldwide are currently enduring a health crisis, as chronic diseases continue to decrease quality of life and promote additional disease states or even death for much of the population. Rural populations are at a particular disadvantage, as they lack access to health clubs, wellness programs and similar resources that are more available in urban areas. Although pharmaceutical therapies have continued to show therapeutic advancements, the rates of disease onset and death from chronic disease has not seen similar improvements, and in fact continue to worsen. Excitingly, significant evidence has been published demonstrating an affordable, effective treatment to directly treat and prevent these chronic diseases, but few have demonstrated successful implementation of this therapy, which is improved lifestyle. Specifically, physical activity and healthy body composition are powerful therapeutics that have been demonstrated to effectively combat and prevent chronic diseases. Additionally, improving these lifestyle factors are often more effective than pharmaceutical interventions without the wide range of side effects. Unfortunately, barriers exist on multiple tiers in the practice of family medicine that demote the implementation of lifestyle medicine. To better serve patients at risk of, or suffering from chronic disease, the investigators are seeking to establish a lifestyle medicine prescription program for rural West Virginia. This program will provide patient education on the benefits of physical activity, body composition, and help patients identify strategies to implement healthy lifestyle choices that can be sustainable for the long-term. Patients will be advised on local opportunities to increase physical activity (yoga studio, martial arts, fitness facilities, aquatic center, etc.) and provided access to the facilities they are most likely to adhere to regularly. They will also be provided training on exercise techniques, equipment, and facilities to increase familiarity and comfort in these settings.

Participants needed: 95
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: West Virginia School of Osteopathic MedicineUpdated: Jul 25, 2025Locations: 1
Eligibility criteria

Program admittance will be restricted to patients with 2+ diagnosed diseases tha... [+1]

no chronic disease diagnosis, lack of physician referral, unwillingness to parti...

Status: Recruiting

The Combined Effect of N-Acetyl Cysteine and Metformin in Polycystic Ovary Syndrome Patients

The study aims to evaluate the effects of combination of metformin with NAC in PCOS on biochemical and hormonal parameters.

Participants needed: 102
Trial details
Phase: Phase 3Age: 20-45Biological sex: FemaleType: InterventionalSponsor: Cairo UniversityUpdated: Jul 9, 2025Locations: 1
Eligibility criteria

Female aged 20 to 45 years old. [+2]

Hypersensitivity to either metformin or NAC. [+14]

Status: Recruiting

Safety of Cultured Allogeneic Adult Umbilical Cord Derived Mesenchymal Stem Cells for PCOS

This trial will study the safety and efficacy of cultured allogeneic adult umbilical cord derived mesenchymal stem cells delivered intravenously for the treatment of Polycystic Ovary Syndrome.

Participants needed: 20
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: The Foundation for Orthopaedics and Regenerative MedicineUpdated: Apr 8, 2025Locations: 2
Eligibility criteria

Active infection [+9]