Viewing Study NCT01671657


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Study NCT ID: NCT01671657
Status: UNKNOWN
Last Update Posted: 2015-10-20
First Post: 2012-08-21
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: US Eeva™ Pregnancy Investigational Clinical Study (US EPIC)
Sponsor: Progyny, Inc.
Organization:

Study Overview

Official Title: US Eeva™ Pregnancy Investigational Clinical Study (US EPIC)
Status: UNKNOWN
Status Verified Date: 2015-10
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: US EPIC
Brief Summary: The purpose of this clinical investigation is to gather data to evaluate the impact of using Eeva with traditional morphology grading on implantation rates.
Detailed Description: The purpose of this clinical investigation is to gather data to evaluate the impact of implantation rates for Day 3 embryo transfers using Eeva and morphology grading (test group) versus Day 3 embryo transfers using morphology grading only (from a concurrent control group).

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?: