Preterm Delivery Risk Prediction by Measurement of Prenatal Serum Screening Markers
Status unconfirmed
Conditions studied: Preterm Delivery
In brief
This protocol seeks to longitudinally collect blood samples from a cohort of pregnant women. The biological specimens will be used to determine the predictive power of biochemical markers routinely used in Down syndrome screening in the assessment of patient's risk of preterm delivery.
Key facts
- Study ID
- NCT01009723
- Run by
- Esoterix Genetic Laboratories, LLC
- People needed
- 2000
- Starts
- 2010-03-01
- Expected to finish
- 2012-07-01
- Last updated by the study team
- 2012-06-08
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- The participant understands the nature of the study and its requirements. To this end, we will require that the participants have command of the English language.
- The participant consents to and signs the approved consent form.
- The participant is 18 years of age or older.
- The participant has a singleton pregnancy.
- The participant is planning on continuing the pregnancy.
- The participant has intent to clinically test for Down syndrome risk.
- The participant consents to the study at the first trimester of her pregnancy.
- The participant understands the nature of the study and its requirements. To this end, we will require that the participants have command of either the English or Spanish language.
You may not qualify if…
- N/A
Where it is running
- Integrated Genetics — Westborough, Massachusetts, United States
- Integrated Genetics — Santa Fe, New Mexico, United States
Full record on ClinicalTrials.gov
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