UCLA Perinatal Biospecimen Repository for pregnancy research

Is this trial a fit for you?

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

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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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.