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UCLA Perinatal Biospecimen Repository

Recruitingn/aAges 1 Minute - anyAllYalda Afshar, MD, PhD
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In plain words

What the trial is, and whether it could suit you

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. Intention to collect perinatal data is aiding the efficiency and effectiveness of de-identified biorepository for pregnancy-at-risk outcome research. The primary aims of the project are: * To design the Case Report Forms (CRFs) for the clinical and biospecimen data. * To create and update the project-specific

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
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.
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What it tests

  • Not listed
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Where

1 site
Afshar Lab, Department of Obstetrics & Gynecology, UCLA
Los Angeles, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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