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