Detailed health profiling for people with PCOS

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project will enroll adult women (18–49 years) who consult the Endocrinology department at CHU de Strasbourg for suspected PCOS or are found to have PCOS during endocrine care. Participants will have standardized collection of medical history, menstrual and reproductive data, hormone measurements including anti-Müllerian hormone (AMH), pelvic ultrasound morphology, and screening for metabolic risk and mood symptoms. No treatments are given as part of the protocol; data will be analyzed to identify clinical and biochemical phenotypes and how they relate to current diagnostic criteria. The aim is to reduce diagnostic delay and clarify feature clusters that could guide more personalized management in the future.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult woman (≥18 years and \<50 years)
* Subject who consulted at the Strasbourg University Hospitals for suspected PCOS or for any other endocrinological condition that led to the discovery of PCOS.

Exclusion Criteria:

* Final diagnosis excluding PCOS.

Where it's running

• ervice d'Endocrinologie, Diabétologie et Nutrition - CHU de Strasbourg - France
  Strasbourg, France Recruiting

Study contacts

• Study coordinator: Thibault BAHOUGNE, MD
• Email: thibault.bahougne@chru-strasbourg.fr
• Phone: 33 3.88.12.78.99

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Using LC-MS/MS to profile androgens for PCOS diagnosis

  This study tests whether LC-MS/MS measurement of androgen profiles can help diagnose PCOS in women compared with healthy controls.

  Recruiting Women's Hospital School Of Medicine Zhejiang University · Hangzhou, Zhejiang · NCT07916909

• Brown adipose tissue responses in PCOS with infrared thermography and inositol

  This study tests whether brown fat activity, measured by infrared skin temperature and UCP-1 levels, differs among women with PCOS (normal weight or overweight/obese) and healthy controls, and whether 12 weeks of inositol changes those responses in overweight/obese PCOS participants.

  Recruiting at 2 sites Istanbul Health and Technology University · Istanbul and 1 other locations · NCT07896642

• Risk tool for blood-clotting problems in adolescents and women with PCOS

  This project will try to build a risk model to spot decreased protein C or S and other clotting abnormalities in females aged 14–45 who have PCOS.

  Recruiting Guangdong Women and Children Hospital · Guangzhou, Guangdong · NCT07571096

• Polycystic Ovary Syndrome in Type 1 Diabetes

  This study tests whether women with type 1 diabetes and PCOS differ from other groups in factors that drive androgen excess and what that means for health.

  Recruiting Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal · Madrid, Madrid · NCT07490964

• PPOS versus GnRH antagonist IVF protocols for women with PCOS

  This trial will test whether a progestin-primed ovarian stimulation (PPOS) protocol or a GnRH antagonist protocol gives better IVF outcomes for women aged 18–40 with PCOS.

  Recruiting Hanoi General Hospital (Vietnam) · Hanoi, Hanoi · NCT07394530

• Tirzepatide for improving reproductive function and metabolic health in overweight women with PCOS

  We will test whether tirzepatide can improve menstrual regularity and metabolic health in premenopausal women with PCOS who are overweight or have obesity.

  Recruiting Phase 4 University of Bonn · Bochum and 1 other locations · NCT07326111

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.