Collection of Maternal Blood Samples for Development of Non-invasive Prenatal Diagnostic Testing
Completed
Conditions studied: Pregnancy Following IVF With PGS/PGD
In brief
The purpose of this study is to collect blood samples from pregnant women who achieved pregnancy following in-vitro fertilization (IVF) with Natera's preimplantation aneuploidy screening (with or without single gene gene testing). These samples will be used for test development of non-invasive prenatal diagnostic testing.
Key facts
- Study ID
- NCT01546324
- Run by
- Natera, Inc.
- People needed
- 16
- Starts
- 2012-02-01
- Expected to finish
- 2013-08-01
- Last updated by the study team
- 2013-08-12
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Pregnant women willing to donate a blood sample during the first or second trimester of their pregnancy (approximately 8-17 weeks gestation)
- Use of Natera (formerly Gene Security Network)'s commercial preimplantation genetic testing (PGS/PGD)to achieve the current pregnancy
You may not qualify if…
- Pregnant women who did not use Natera (formerly Gene Security Network)'s PGS/PGD testing to achieve their current pregnancy
Where it is running
- Natera, Inc — Redwood City, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.