Eeva™ Pregnancy Investigational Clinical Study: A Postmarket Follow-Up Study

NCT01671644 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 104

Last updated 2015-10-20

No results posted yet for this study

Summary

The purpose of this postmarket study is to gather data to evaluate the impact of using Eeva with traditional morphology grading on clinical pregnancy rates.

Conditions

Sponsors & Collaborators

  • Progyny, Inc.

    lead INDUSTRY

Principal Investigators

  • Shehua Shen, MD, ELD · Progyny, Inc.

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2015-06-30
Completion
2015-10-31

Countries

  • Belgium
  • Netherlands

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01671644 on ClinicalTrials.gov