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Intrauterine G-CSF Administration in RIF — G-CSF  

Infertility Clinical Trial

Official title:
Intrauterine G-CSF Administration in Recurrent Implantation Failure

Clinical Trial Summary

Aim of this study is to investigate the effects of intrauterine G-CSF on endometrial thickness, clinical pregnancy rate and live birth rate in a recurrent implantation failure (RIF) group

Clinical Trial Description

This study was designed as a prospective randomized controlled trial with the involvement of 200 RIF group patients.The procedure will perform by administering 30 mIU of Leucostim®(Filgrastim [G-CSF] 30mIU/mL; DEM Medical, Dong-A; South Korea) through slow infusion into the endometrial cavity using a soft embryo transfer catheter. Normal saline of 1 mL will be infused into the endometrial cavity in the same way in the control group. The standard ICSI procedure will use for all patients, and fresh cycle embryos will be transferred on the third or fifth day. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03783208
Study type Interventional
Source Gurgan Clinic
Contact
Status Completed
Phase N/A
Start date November 1, 2018
Completion date December 20, 2018
View Details
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