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Search / Trial NCT00492882

Study of Mechanisms of Anovulation in Polycystic Ovary Syndrome

Launched by UNIVERSITY HOSPITAL, LILLE · Jun 26, 2007

Trial Information

Current as of May 20, 2025

Completed

Keywords

Polycystic Ovary Syndrome Follicular Arrest Anti Mullerian Hormone Fsh

ClinConnect Summary

Women with PCOS (Rotterdam definition) whom anovulation is resistant to clomiphene citrate will receive recombinant FSH using the low-dose step-up protocol during only one cycle. Serum levels of estradiol, AMH, LH, FSH, inhibin B and ultrasound (U/S) parameters will be assessed twice a week until 3 days after appearance of \> 1 dominant follicle(s).The starting dose of recFSH will be 50 IU/day. In the absence of criteria for dominance (see below) after 14 days at 50 IU/day, recFSH dose will be increased by 25 IU/day every 7 days until dominance is achieved. Dominance will be defined by the ...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • normal sperm analysis in the partners and normal hysterosalpingography in all patients
  • PCOS defined by Rotterdam criteria
  • resistance to clomiphene citrate, i.e. no ovulation at 150 mg/day or no pregnancy after 6 ovulatory cycles
  • informed consent before inclusion
  • Exclusion Criteria:
  • on-going pregnancy
  • age\<18 or \>40 yr.
  • unability to understand the treatment protocol
  • other medications
  • any co-existent morbid condition contra-indicating a pregnancy

About University Hospital, Lille

University Hospital Lille is a leading academic medical institution dedicated to advancing healthcare through innovative clinical research and patient-centered care. As a prominent sponsor of clinical trials, the hospital leverages its extensive resources, multidisciplinary expertise, and state-of-the-art facilities to facilitate groundbreaking studies across various medical fields. Committed to enhancing therapeutic options and improving patient outcomes, University Hospital Lille collaborates with researchers, healthcare professionals, and industry partners to ensure rigorous scientific standards and ethical practices in all clinical trials.

Locations

Lille Cedex, , France

Patients applied

0 patients applied

Trial Officials

Didier R DEWAILLY, MD

Study Chair

University Hospital of Lille

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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