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NCT06339606Not yet recruiting

Pregnancy Repository

Repository for Biospecimens From Pregnant Patients

Source: ClinicalTrials.gov · Last updated 24 Apr 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

An essential part of clinical research is the availability and accessibility of human biospecimens for the identification of biomarkers, new treatments and measurement of response to therapy. Proteins, RNA and DNA can be extracted and studied as well. This is a critical first step in performing many fundamental molecular biology experiments. A variety of biospecimens are utilized for research including but not limited to normal and malignant tissues, blood, and other body fluids. In order to obtain high-quality biospecimens, they must be acquired serially, stored according to current standards, and matched with clinical information for maximum value. As such, the investigators would like to create a repository of biospecimens collected from pregnant patients who are seen at Mount Sinai Hospital and other research hospitals in Toronto. Mount Sinai provides personnel and infrastructure to serve the largest (7500 births/year) and highest complex Maternity program in Ontario. Of the 7500 patients a year, at least 2500 are considered high risk pregnancies, where there's a possibility of preeclampsia, placenta accreta and a host of other complications. For this study, biological specimens - blood, cervical and placental samples - will be collected from these high-risk groups in order to better understand the causes of the underlying conditions.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
7000 (estimated)
First submitted
15 Mar 2024
Start date
1 May 2024
Primary completion date
30 Apr 2026
Lead sponsor
Sunnybrook Health Sciences Centre
NCT number
NCT06339606

What you commit to

  • Study type: Observational
  • Planned participants: 7000
  • From 1 May 2024 to the primary completion date, 30 Apr 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None

Who the study is looking for

  • Consenting pregnant adults (age 18-45 years) with known or suspected risk for abnormal placentation (Abnormal Placentation Group)
  • Consenting pregnant adults (age 18-45 years) with low-risk pregnancies (Control Group)
  • Singleton or multiple pregnancy
  • Ongoing clinical care at the participating sites, with delivery at the same institution.

Age in the registry: 18 years to 45 years · Sex: Female

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.