Evaluation of the Efficacy of Diafert in Predicting Embryos' Potential to Develop to the Blastocyst Stage
Completed
Conditions studied: Infertility
In brief
This prospective study will evaluate the efficacy of Diafert as an adjunct to morphological assessment in predicting embryos' potential to develop to the blastocyst stage on Day 5.
Key facts
- Study ID
- NCT02788617
- Run by
- Forest Laboratories
- People needed
- 100
- Starts
- 2016-06-24
- Expected to finish
- 2017-04-04
- Last updated by the study team
- 2017-07-31
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Provide written informed consent before initiation of any study procedures
- Be a female outpatient, ≥ 18 years of age at the time of informed consent
- Have at minimum 10 mature egg follicles as of the last transvaginal ultrasound following hormonal stimulation
- Eligible to allow embryos to develop through day 5 before implantation or freezing
You may not qualify if…
- Presence of ovarian endometriotic cyst
- Presence or history of diagnosed severe endometriosis (i.e. stage IV the revised American Fertility Society classification for endometriosis).
- Need for pre-implantation genetic diagnosis/screening of embryos
- Use of time-lapse embryo imaging
- Employee or immediate relative of an employee of Forest Research Institute, Inc., any of its affiliates or partners, or the study center
Where it is running
- Huntington Reproductive Center — Encino, California, United States
- Women's Medical Research Group — Clearwater, Florida, United States
- InVia Fertility Specialists — Hoffman Estates, Illinois, United States
- Institute for Reproductive Health — Cincinnati, Ohio, United States
- Main Line Fertility Center — Bryn Mawr, Pennsylvania, United States
- Dallas - Fort Worth Fertility Associates — Dallas, Texas, United States
- Houston Fertility Institute — Houston, Texas, United States
- Utah Fertiity Center — Pleasant Grove, Utah, United States
- Reproductive Care Center — Sandy City, Utah, United States
Full record on ClinicalTrials.gov
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