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Eeva™ Continued Access Study: Assessing the Usability of Eeva in a Clinical Setting

NCT01617993 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2014-01-13

No results posted yet for this study

Summary

User questionnaire of Eeva System usability and reports of device malfunctions.

Conditions

Sponsors & Collaborators

  • Progyny, Inc.

    lead INDUSTRY

Principal Investigators

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

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • United States

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 NCT01617993 on ClinicalTrials.gov