Correlating Time-Lapse Parameters Detected by the Eeva™ System With Comprehensive Chromosome Screening Results
NCT01635049 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 110
Last updated 2015-01-14
Summary
The purpose of this research study protocol is to collect imaging data on embryos followed to blastocyst stage (Day 5-6) and correlate Eeva System parameters with comprehensive chromosome screening (CCS) results, implantation and live birth.
Conditions
Sponsors & Collaborators
-
Progyny, Inc.
lead INDUSTRY
Principal Investigators
-
Richard T Scott, Jr., MD · Reproductive Medicine Associates of New Jersey
Eligibility
- Max Age
- 43 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-06-30
- Primary Completion
- 2014-12-31
- Completion
- 2014-12-31
Countries
- United States
Study Locations
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