Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

Biobank for studying pregnancy complications like preeclampsia and preterm birth

Official title: Biobank of Data and of Human Biological Samples on Prematurity, Preeclampsia and Other Pregnancy Complications

Run by CHU de Quebec-Universite Laval · NCT02744365 · Data updated 2026-11-12

This study collects samples and information from pregnant women to see if it can help identify the causes of complications like preeclampsia and preterm birth.

More Preeclampsia trials

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment7845 (estimated)
SponsorCHU de Quebec-Universite Laval
Academic / other
Locations1 site (Québec)
StatusRecruiting
StartedApril 2015
Main results expectedApril 2025
Study endsApril 2028
Registry record updatedMarch 16, 2022
Trial IDNCT02744365 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are pregnant women who are able to provide informed consent and meet specific inclusion criteria from the original studies.

Probably not a fit

Patients who are under 18 years old, have a negative fetal heart rate at recruitment, or cannot provide informed consent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This biobank collects and stores data and biological samples from women participating in various studies related to pregnancy complications, including preeclampsia and preterm birth. It includes medical, social, obstetrical, and ultrasonographic data, as well as human biological samples such as maternal plasma and cord blood. The goal is to analyze these samples and data to identify risk factors and markers associated with pregnancy complications. This observational approach allows for a comprehensive understanding of the conditions affecting pregnancy outcomes.

Why it matters

Potential benefit: If successful, this biobank could lead to improved prediction and management of pregnancy complications, enhancing maternal and fetal health.

How similar studies have gone: Other studies focusing on biobanks for pregnancy complications have shown promise in identifying risk factors and improving outcomes, suggesting this approach is supported by previous successes.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • CHU de Quebec
    Québec, Canada
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.