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

Completed

Conditions studied: Infertility

In brief

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

Key facts

Study ID

NCT01617993

Run by

Progyny, Inc.

People needed

31

Starts

2012-06-01

Expected to finish

2013-02-01

Last updated by the study team

2014-01-13

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 or donor eggs
• Subject is ≥ 18 and ≤ 40 years of age.
• Subject has basal antral follicle count (AFC) ≥ 8 prior to stimulation cycle.
• Fertilization using only ejaculated sperm (fresh or frozen) - no surgically retrieved sperm.
• Subject has ≥ 5 normally fertilized eggs (2 PN)
• Willing to have all 2PN embryos monitored by Eeva
• Willing to comply with study protocol and procedures and able to speak English.
• Willing to provide written informed consent.

You may not qualify if…

• Reinseminated eggs.
• History of cancer.
• Gestational carriers.
• Planned preimplantation genetic diagnosis or preimplantation genetic screening.
• Previously enrolled in this study
• Concurrent participation in another clinical study.

Where it is running

• Pacific Fertility Center — San Francisco, California, United States
• Fertility Physicians of Northern California — San Jose, California, United States
• Reproductive Science Center — San Ramon, California, United States

Full record on ClinicalTrials.gov

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