Blood Samples for Preeclampsia Screening
Non-Invasive Preeclampsia Screening and Biobank
Recruiting
Observational Study
Preeclampsia (PE)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Observational
- Participants needed
- 6,550 (estimated)
- Sponsor
- Sequenom, Inc. · Industry
Who this trial is looking for
This trial is looking for women who are between 11 and 14 weeks pregnant. Participants will provide blood samples to help test for a condition called preeclampsia.
Are You a Good Fit for This Trial?
You may be able to join if
- I am a woman aged 18 or older.
- I am pregnant with one baby and between 11 and 14 weeks along.
- I can provide my health records and test results.
- I agree to have certain tests done during my ultrasound visits.
- I will provide blood samples during each trimester visit.
- I agree to share my pregnancy and health information.
You may not be able to join if
- I might not return for later tests in my pregnancy.
- I might not have my pregnancy outcome data available.
- I have donated a sample for this trial with the same pregnancy before.
- I am taking part in a study with blinded aspirin or I do not know what dose of aspirin I am taking.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
Women pregnant between 11-14 weeks gestation will be enrolled with blood samples collected to evaluate for preeclampsia.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Subject is female and 18 years of age and older;
* Subject provides a signed and dated informed consent;
* Subject is pregnant with a singleton pregnancy at ≥11.0 - ≤14.0 weeks' gestation;
* Subject agrees to provide the Sponsor access to any prenatal and postnatal screening o…
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