Antagonist Protocol in IVF
Phase 2
- Conditions
- Infertility
- Interventions
- Drug: Gonadotropins releasing hormone antagonist
- Registration Number
- NCT02335736
- Lead Sponsor
- Woman's Health University Hospital, Egypt
- Brief Summary
The antagonist protocol in a novel method of stimulation in the in vitro fertilization (IVF) patients. It has been tried in poor responders, polycystic ovary (PCO) patients and normal females undergoing IVF. Can it be used with the same efficacy in all patients?
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
- age: 20- 44 years
- Poor responder females according to Bologna criteria
- Polycystic ovarian disease females according to Rotterdam criteria
- Females with infertility causes other than poor responders, or PCO; male factor or tubal block
Exclusion Criteria
- refusal to get enrolled in the study
- cases of infertility due to severe male factor
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Normal Gonadotropins releasing hormone antagonist Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant (Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC. Poor responders Gonadotropins releasing hormone antagonist Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant (Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC Polycystic ovarian disease Gonadotropins releasing hormone antagonist Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant(Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC
- Primary Outcome Measures
Name Time Method number of oocytes collected and fertilized 6 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Kasr el aini hospital
🇪🇬Cairo, Egypt