US Eeva™ Pregnancy Investigational Clinical Study (US EPIC)

Status unconfirmed

Conditions studied: Infertility

In brief

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

Key facts

Study ID

NCT01671657

Run by

Progyny, Inc.

People needed

100

Starts

2013-01-01

Expected to finish

2016-06-01

Last updated by the study team

2015-10-20

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women undergoing fresh in vitro fertilization treatment using their own eggs or donor eggs.
• IVF cycle attempts ≤ 2.
• Egg age ≤ 40 years.
• Planned Day 3 embryo transfer.
• At least 4 normally fertilized eggs (2PN).
• All 2PN embryos must be imaged by Eeva.
• Ejaculated sperm or sperm from the epididymis (fresh or frozen).
• Willing to comply with study protocol and procedures.
• Willing to provide written informed consent.

You may not qualify if…

• Planned preimplantation genetic diagnosis or preimplantation genetic screening.
• Planned "freeze all" cycle (oocytes or embryos).
• Sperm retrieved from testicular tissue.
• Abnormal uterine cavity as evaluated by standard methods.
• Gestational carrier.
• Endometriosis
• Hydrosalpinx.
• History of cancer.
• Concurrent participation in another clinical study.

Where it is running

• Fertility Physicians of Northern California — San Jose, California, United States

Full record on ClinicalTrials.gov

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