Biobank on Prematurity, Preeclampsia and Other Pregnancy Complications
Recruiting
Observational Study
Preeclampsia
Preterm Birth
Pregnancy Complications
Fetal Anomalies
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
- 7,845 (estimated)
- Sponsor
- CHU de Quebec-Universite Laval · Other
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About This Trial
The Biobank includes data and biological specimens of women from three original studies: 1) First-trimester Prediction of Preeclampsia (PREDICTION Study, NCT02189148), 2) Pre-Eclampsia And growth Retardation, an evaluative Longitudinal study (PEARL Study, NCT02379832), 3) Effect of Low Dose Aspirin on Birthweight in Twins: The GAP Trial (NCT02280031) and 4)PREDICTION2: Prediction of Preeclampsia a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* (specific to each study)
Exclusion Criteria:
* pregnant women \<18 years old at recruitment
* negative fetal heart at recruitment
* women not able to provide an informed consent to the study
Contacts