UCLA Perinatal Biospecimen Repository

Recruiting Observational Study
Pregnancy High-Risk Pregnancy
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
1 Minute and older
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
Yalda Afshar, MD, PhD · Other
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About This Trial
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), …
Trial Locations
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Eligibility 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 gi…
Contacts

Yalda Afshar, MD. PhD

(805) 338-5593

yafshar@mednet.ucla.edu

CONTACT

Jenny Lester, BS

323-428-2338

jlester@mednet.ucla.edu

CONTACT