Correlating Time-Lapse Parameters With aCGH Testing in IVF Treatment (aCGH Study)



Status:Active, not recruiting
Conditions:Women's Studies, Infertility
Therapuetic Areas:Reproductive
Healthy:No
Age Range:18 - 43
Updated:4/21/2016
Start Date:May 2014
End Date:February 2016

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Trial Summary
Trial Overview
Inclusion Criteria

Correlating Time-Lapse Parameters Detected by Eeva™ With Array-Comparative Genomic Hybridization Results and Ongoing Pregnancy Rates (aCGH Study)

The purpose of this research study protocol is to collect imaging data on embryos followed
to blastocyst stage (Day 5-6) and correlate Eeva parameters with array - Comparative Genomic
Hybridization (aCGH) results and ongoing pregnancy rates.

The present study was designed to determine if there is a correlation between the Eeva
System parameters and aCGH testing results. Embryos will be selected for transfer based on
aCGH results and morphology. The Clinical site will have no access to the Eeva analysis at
the time of the transfer.

Inclusion Criteria:

- Subject is ≤43 years of age.

- Women undergoing IVF treatment with planned aCGH testing using her own eggs or donor
eggs.

- Antral Follicle Count ≥ 6 at time of cycle start

- Baseline (day 2-3 of cycling) FSH ≤ 15 mIU/ml

- Antimüllerian Hormone level ≥ 0.5 ng/mL

- Fertilization using only ejaculated sperm (fresh or frozen) - no surgically retrieved
sperm.

- Willing to have all 2PN embryos monitored by Eeva

- Not previously enrolled in this study.

- Willing to comply with study protocol and procedures and able to speak English.

- Willing to provide written informed consent.

Exclusion Criteria:

- BMI ≥ 40

- Prior IVF cycle with < 4 x 2PN

- Planned Day 3 Assisted Hatching
We found this trial at
1
site
Main Line Fertility
Bryn Mawr, Pennsylvania 19010
?
mi
from
Bryn Mawr, PA
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