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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
GroupInterventionDescription
NormalGonadotropins releasing hormone antagonistHuman 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 respondersGonadotropins releasing hormone antagonistHuman 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 diseaseGonadotropins releasing hormone antagonistHuman 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
NameTimeMethod
number of oocytes collected and fertilized6 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kasr el aini hospital

🇪🇬

Cairo, Egypt

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