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Time-lapse enabled embryo test
Day 3 eSET combined with Eeva for Infertility (PPS Trial)
N/A
Waitlist Available
Research Sponsored by Progyny, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8-12 week gestation
Awards & highlights
PPS Trial Summary
The purpose of this clinical investigation is to gather pilot data to evaluate the impact of using Eeva™, a time-lapse enabled embryo test, in combination with traditional morphology on clinical pregnancy rates.
PPS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8-12 week gestation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8-12 week gestation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Clinical Pregnancy
Secondary outcome measures
Ongoing pregnancy rate
PPS Trial Design
3Treatment groups
Active Control
Group I: Day 3 eSET combined with EevaActive Control1 Intervention
Traditional Morphology + Eeva™ results
Group II: Day 5 eSET with Traditonal MorphologyActive Control1 Intervention
Group III: Day 5 eSET combined with EevaActive Control1 Intervention
Traditional Morphology + Eeva™ results
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Who is running the clinical trial?
Progyny, Inc.Lead Sponsor
9 Previous Clinical Trials
2,272 Total Patients Enrolled
9 Trials studying Infertility
2,272 Patients Enrolled for Infertility
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