Viewing Study NCT01816802


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Study NCT ID: NCT01816802
Status: UNKNOWN
Last Update Posted: 2015-03-26
First Post: 2013-03-20
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Registry Study of Traditional Morphology Grading Combined With Eeva in IVF Treatment
Sponsor: Progyny, Inc.
Organization:

Study Overview

Official Title: MERGE: MulticEnter ReGistry With Eeva
Status: UNKNOWN
Status Verified Date: 2015-03
Last Known Status: ACTIVE_NOT_RECRUITING
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: MERGE
Brief Summary: The purpose of this study is to record and evaluate the use of traditional morphology grading combined with Eeva in the treatment of in vitro fertilization.
Detailed Description: This is a prospective, observational, single-arm, nonrandomized, multicenter study. Data will be collected to establish eligibility, at baseline, during the stimulation and in vitro fertilization process, during embryo culture, at embryo transfer, at 12-18 days post egg retrieval to verify biochemical pregnancy, and then typically at 5-6 weeks gestational weeks to verify clinical pregnancy.

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
TST 2193-p OTHER Auxogyn View