Viewing Study NCT00504530



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Last Modification Date: 2024-10-26 @ 9:34 AM
Study NCT ID: NCT00504530
Status: COMPLETED
Last Update Posted: 2017-01-04
First Post: 2007-07-18

Brief Title: r-hLIF for Improving Embryo Implantation in IVF
Sponsor: Merck KGaA Darmstadt Germany
Organization: Merck KGaA Darmstadt Germany

Study Overview

Official Title: A Randomised Double-blind Placebo Controlled Proof of Concept Study to Assess the Efficacy Safety and Acceptability of r-hLIF for Improving Embryo Implantation Following in Vitro Fertilisation IVF and Embryo Transfer ET in Women With Recurrent Implantation Failure
Status: COMPLETED
Status Verified Date: 2016-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study was designed to obtain pilot clinical evidence of the efficacy safety and acceptability of r-hLIF administered during the luteal phase after IVFintra-cytoplasmic sperm injection ICSI and ET for improving embryo implantation in infertile women with a history of at least three implantation failures following ART Based on LIF expression patterns and experimental data from animal research a role of LIF in embryo implantation is anticipated
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None