Registry Study of Traditional Morphology Grading Combined With Eeva in IVF Treatment (MERGE)

Progyny

Status: Unknown

Conditions: Infertility

Treatments: Device: In-vitro fertilization using Eeva

Study type: Observational

Funder types: Industry

Identifiers

NCT01816802

2012-AUX-009

TST 2193-p (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to record and evaluate the use of traditional morphology grading combined with Eeva in the treatment of in vitro fertilization.

Full description

This is a prospective, observational, single-arm, nonrandomized, multicenter study. Data will be collected to establish eligibility, at baseline, during the stimulation and in vitro fertilization process, during embryo culture, at embryo transfer, at 12-18 days post egg retrieval to verify biochemical pregnancy, and then typically at 5-6 weeks gestational weeks to verify clinical pregnancy.

Enrollment: 1,200 estimated patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• women undergoing fresh in vitro fertilization treatment using their own eggs or donor eggs.

Exclusion criteria

• history of cancer.
• gestational carrier.

Trial design

1,200 participants in 1 patient group

In-vitro fertilization using Eeva

Description:

Patients undergoing in-vitro fertilization treatment who provide informed consent and use Eeva in their treatment cycle.

Treatment:

Device: In-vitro fertilization using Eeva