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

Progyny

Status: Completed

Conditions: Infertility

Study type: Observational

Funder types: Industry

Identifiers

NCT01617993

2012-AUX-002

Details and patient eligibility

About

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

Full description

This study is designed to evaluate the use of Eeva by IVF laboratory staff during routine procedures. The fertilized eggs will be placed in an Eeva dish and the development of the embryos will be monitored by the Eeva system in a standard incubator. On day 3 of embryo culture, Eeva blastocyst prediction data will be printed from the system to be used to assist the embryologist in selecting the best embryo(s). The performance of the system will be summarized and the user feedback from the embryologists will be collected.

Enrollment: 31 patients

Sex: Female

Ages: 18 to 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Trial design

31 participants in 1 patient group

Women undergoing IVF treatment

Description:

Women undergoing IVF treatment