Status:
UNKNOWN
The Psychological and Social Impact of PCOS
Lead Sponsor:
University Hospital, Lille
Conditions:
Polycystic Ovary Syndrome
Eligibility:
FEMALE
18+ years
Brief Summary
The aim of the study is to assess the association between the quality of life of patients with PCOS and various factors (age, BMI, socio-professional category, delay in diagnostic of PCOS, infertility...
Eligibility Criteria
Inclusion
- Female sex
- Adult patient (aged 18 or over)
- Able to read and write in French
- diagnosed at a previous consultation as having PCOS according to the Rotterdam criteria (at least 2 out of 3 criteria from:
- Clinical signs of hyperandrogenism (hirsutism, acne, androgenic alopecia) and/or biochemical signs of hyperandrogenism (total testosterone \> 0.39 ng/mL and/or androstenedione \> 1.75 ng/mL)
- Ovulation disorders (infertility, oligomenorrhoea or amenorrhoea or cycle length either \<21 days or \>35 days),
- Polymicrocystic ovaries on ultrasound (either 19 or more follicles measuring 2-9 mm in diameter and/or increased ovarian volume (\>10 cm3) and/or increased ovarian area (\> 5.5 cm²) without presence of cyst or dominant follicle.)
- Informed consent
Exclusion
- Patient with no health insurance cover
- Difficulties understanding or speaking French
- Computer (tablet/smartphone) and internet connection required.
- Refusal to take part in research
- Under court protection (guardianship/curatorship/privation of liberty)
Key Trial Info
Start Date :
July 7 2023
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
April 7 2024
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT05982236
Start Date
July 7 2023
End Date
April 7 2024
Last Update
August 25 2023
Active Locations (1)
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1
CHU de Lille Hôpital Jeanne de Flandre
Lille, Nord, France, 59000