UCLA Perinatal Biospecimen Repository for pregnancy research
UCLA Perinatal Biospecimen Repository
This study is collecting and storing blood and tissue samples from pregnant women to help researchers learn more about pregnancy-related health issues.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 1 Minute and up |
| Sex | All |
| Sponsor | University of California, Los Angeles Academic / other |
| Locations | 1 site (Los Angeles, California) |
| Trial ID | NCT05035160 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to establish the UCLA Perinatal Biospecimen Repository, which will collect, store, and distribute clinical data and biological specimens from participants with perinatal pathology. The study will involve approximately 500 participants over a duration of 5 years, with data collection occurring from one to six visits. Core variables of interest include clinical characteristics and various biological samples such as maternal blood, cord blood, and placenta. The repository will serve as a high-quality resource for research on pregnancy-related outcomes.
Who should consider this trial
Good fit: Ideal candidates include pregnant and postpartum individuals aged 18 and over with perinatal pathology, as well as healthy pregnant and postpartum individuals and healthy non-pregnant volunteers.
Not a fit: Patients who are unwilling to provide written informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this repository could enhance research on high-risk pregnancies and improve outcomes for both mothers and infants.
How similar studies have performed: Other studies utilizing biospecimen repositories for pregnancy research have shown promise, indicating that this approach is both relevant and beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Pregnant and postpartum birthing persons aged 18 and over with perinatal pathology; * Healthy pregnant and postpartum birthing persons; * Healthy non-pregnant birthing persons (healthy volunteers). Exclusion Criteria: * Pregnant and postpartum birthing person unwilling to give written informed consent to participate in the study.
Where this trial is running
Los Angeles, California
- Afshar Lab, Department of Obstetrics & Gynecology, UCLA — Los Angeles, California, United States (Recruiting)
Study contacts
- Principal investigator: Yalda Afshar, MD, PhD, MD. PHD — University of California, Los Angeles
- Study coordinator: Yalda Afshar, MD. PhD
- Email: yafshar@mednet.ucla.edu
- Phone: (805) 338-5593
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.