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UCLA Perinatal Biospecimen Repository

NCT05035160

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this investigator-initiated prospective observational cohort study is to establish the new UCLA Perinatal Biospecimen Repository (Perinatal Repository) for collection, storage, and distribution of the human data and biospecimens of the participants with perinatal pathology. The secure and shared high-quality resource of clinical data and biological specimens (Repository Materials), across pregnancy pathology related to research protocols at the Afshar's Lab will be created. Core variables of interest include clinical characteristics and relevant biological samples.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Pregnancy
  • High-Risk Pregnancy

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
1 Minute and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Yalda Afshar, MD, PhD
Last updated on ClinicalTrials.gov
December 29, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • Afshar Lab, Department of Obstetrics & Gynecology, UCLA · Los Angeles, CA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.