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The Value of Addition of Human Menopausal Gonadotropin Drug Following Oocytes Retrieval in IVF Cycles

Infertility Clinical Trial

Official title:
Human Menopausal Gonadotropin as a Novel Addition to Luteal Phase Support in Down-regulated ICSI Cycles (RCT)

Clinical Trial Summary

The aim of this study is to test the hypothesis that addition of daily small dose of human menopausal gonadotropin (HMG) drug following oocytes retrieval could improve the fertility outcome in women undergoing in-vitro fertilization

Clinical Trial Description

The study will be conducted in the IVF unit of Cairo University. Females undergoing ICSI cycles in the age between 20 and 40 years will be allocated to one of 2 groups. Long agonist protocol will be used. Allocation to either one of 2 groups will be done on the day of oocytes retrieval. The first group will take (in addition to the routine care) daily human menopausal gonadotropin drug injection for 2 weeks. The second group will receive the routine care. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03209687
Study type Interventional
Source Cairo University
Contact Eman Omran, M.D.
Phone 00223682030
Email eman.omran@kasralaini.edu.eg
Status Recruiting
Phase Phase 4
Start date July 6, 2017
Completion date August 15, 2024
View Details
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