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Assessment of the Impact of Polycystic Ovary Syndrome on Women's Sexuality (SexOPK)

T

Toulouse University Hospital

Status

Completed

Conditions

Polycystic Ovarian Syndrome (PCOS)

Treatments

Other: women answer a questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT06887296
ID-RCB : 2025-A00613-46 (Other Identifier)
RC31/25/0135

Details and patient eligibility

About

This study, titled SexOPK, aims to evaluate the impact of polycystic ovary syndrome (PCOS) on women's sexual health. PCOS is a common endocrine disorder affecting 5-20% of women of reproductive age, often leading to hormonal imbalances, metabolic issues, and psychological distress. Despite existing studies on the subject, the level of sexual distress associated with PCOS-related sexual dysfunction remains unclear.

The study will compare sexual function and distress levels between women diagnosed with PCOS and a control group without PCOS. Participants will complete an online questionnaire assessing various aspects of sexual health, body image, anxiety, and depression. The findings may help healthcare professionals better understand and address sexual dysfunction in women with PCOS.

Enrollment

84 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For patients in the test group (PCOS):

  • Adults
  • Carriers of medically diagnosed polycystic ovarian syndrome
  • Non-opposition

For patients in the control group:

  • Adults
  • Not carriers of polycystic ovarian syndrome
  • Unopposed

Exclusion criteria

  • Patient under court protection, guardianship, or curatorship
  • Does not understand or speak French

Trial design

84 participants in 2 patient groups

Women with polycystic ovary syndrome
Treatment:
Other: women answer a questionnaire
Women without polycystic ovary syndrome
Treatment:
Other: women answer a questionnaire

Trial contacts and locations

1

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Central trial contact

Caroline Peyrot, CRA

Data sourced from clinicaltrials.gov

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