Eeva™ Pregnancy Pilot Study (PPS)

Status unconfirmed · Not applicable

Conditions studied: Infertility

In brief

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.

Key facts

Study ID

NCT02218255

Run by

Progyny, Inc.

People needed

240

Starts

2014-08-01

Expected to finish

2016-06-01

Last updated by the study team

2015-10-20

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women undergoing fresh in vitro fertilization treatment using their own eggs
• ≤ 40 years
• ≥ 4 diploid embryos (i.e. having 2 PNs)
• ≤ 3 Prior ART cycles (IVF, ICSI and related procedures)
• All 2PN embryos (for all 3 arms) must be imaged by Eeva
• Subject willing to comply with study protocol and procedures
• Subject willing to provide written informed consent

You may not qualify if…

• Preimplantation genetic diagnosis or preimplantation genetic screening
• Planned "freeze all" cycle (eggs or embryos)
• Asherman's Syndrome
• Donor egg
• Gestational carrier
• Presence of Hydrosalpinx on ultrasound
• Concurrent participation in an interventional clinical study

Where it is running

• Brigham and Women's Hospital — Boston, Massachusetts, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.