GnRHa for Luteal Phase Support in Long GnRHa Protocol Cycles

Status Recruiting

Clinical Trial Summary

Evaluation of the effect of adding a single dose of gonadotropin releasing hormone agonist (GnRHa) as a luteal phase support on the outcomes of intracytoplasmic sperm injection (ICSI) following long GnRHa protocol

Clinical Trial Description

Endometrial preparation for embryo transfer (ET) will be started after oocyte retrieval by giving 800 mg/day natural progesterone vaginal supplement + 4 mg/day estradiol oral supplement. The patients will be randomly divided into 2 groups for luteal phase support: (i) Group A (GnRHa group) in which the luteal phase support will be continued by the same regimen started on the day of oocytes retrieval until 2 weeks after embryo transfer (ET) with subcutaneous administration of a single dose (0.2 mg) of GnRHa (Triptorelin) 6 days after oocyte retrieval, and (ii) Group B (control group) in which the luteal phase support will be continued only by the same regimen started on the day of oocytes retrieval until 2 weeks after ET ;

Study Design

Related Conditions & MeSH terms

Infertility

Clinical Trial Details

NCT number	NCT02312076
Study type	Interventional
Source	Mansoura University
Contact	Mohamed S Abdelhafez, Dr
Phone	+201144523366
Email	msabdelhafez@gmail.com
Status	Recruiting
Phase	Phase 4
Start date	September 9, 2016
Completion date	December 31, 2024

View Details

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