Trial Information
Ovarian Stimulation and Intrauterine Insemination in Women With Polycystic Ovarian Syndrome
Inclusion Criteria:
- women who failed to get pregnant after 6 ovulation induction cycles with clomiphene
citrate (cc) alone, despite of being ovulating with cc, having patent Fallopian tubes as
confirmed by hysterosalpingography and their partners had fertile semen parameters
according to criteria of World Health Organization (WHO 2010)
Exclusion Criteria:
male factor infertility
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Outcome Measure:
Live Birth Rate
Outcome Time Frame:
20 months
Safety Issue:
No
Principal Investigator
Ahmed Gibreel, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Mansoura University
Authority:
Egypt: Ministry of Higher Education
Study ID:
AG/4/2010
NCT ID:
NCT01675843
Start Date:
May 2010
Completion Date:
Related Keywords:
- Infertility
- Polycystic Ovarian Syndrome
- Intrauterine Insemination
- Infertility
- PCOS
- IUI
- Infertility
- Polycystic Ovary Syndrome