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Antagonist Protocol in IVF

W

Woman's Health University Hospital, Egypt

Status and phase

Unknown
Phase 2

Conditions

Infertility

Treatments

Drug: Gonadotropins releasing hormone antagonist

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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?

Enrollment

200 estimated patients

Sex

Female

Ages

20 to 44 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 3 patient groups

Normal
Active Comparator group
Description:
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.
Treatment:
Drug: Gonadotropins releasing hormone antagonist
Poor responders
Active Comparator group
Description:
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
Treatment:
Drug: Gonadotropins releasing hormone antagonist
Polycystic ovarian disease
Active Comparator group
Description:
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
Treatment:
Drug: Gonadotropins releasing hormone antagonist

Trial contacts and locations

1

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Central trial contact

Dina M Dakhly, MD; mohamed abdalla, MD

Data sourced from clinicaltrials.gov

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