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Spots Global Cancer Trial Database for Letrozole or Laparoscopic Ovarian Diathermy for Women With CC Resistant Polycystic Ovary Syndrome.

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Trial Identification

Brief Title: Letrozole or Laparoscopic Ovarian Diathermy for Women With CC Resistant Polycystic Ovary Syndrome.

Official Title: Letrozole Versus Laparoscopic Ovarian Diathermy for Ovulation Induction in Clomiphene-resistant Women With Polycystic Ovary Syndrome

Study ID: NCT00956267

Study Description

Brief Summary: The purpose of this study is to compare and determine the efficacy of letrozole administration to that of laparoscopic ovarian diathermy (LOD) in infertile women with Polycystic ovary syndrome(PCOS)not responding to treatment with Clomiphene alone.

Detailed Description: In the letrozole group, withdrawal bleeding was achieved using 10 mg of dydrogesterone tablets for 10 days before stimulation, then 2.5 mg of letrozole oral tablets (Femara; Novartis Pharma Services, Switzerland) daily from day 3 of the menses for 5 days up to six cycles. All patients in the control group underwent laparoscopic ovarian diathermy, then followed up for 6 months.

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Mansoura University Hospitals,OB/GYN department, Mansoura, Dakahlia Governorate, Egypt

Contact Details

Name: Hatem Abu Hashim, MD. MRCOG

Affiliation: Mansoura University Hospital

Role: PRINCIPAL_INVESTIGATOR

Name: Abdel Maged Mashaly, MD

Affiliation: Mansoura University Hospital

Role: STUDY_DIRECTOR

Name: Ahmed Badawy, MD.PhD.

Affiliation: Mansoura University Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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