Recruiting

Perinatal Biospecimen

Sponsor:

Yalda Afshar, MD, PhD

Code:

NCT05035160

Conditions

Pregnancy

High-Risk Pregnancy

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

Study Details

Brief 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. 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 policies, agreements, and Standard Operating Procedures (SOPs).
  • To develop the data management system to assure personal health information de-identification, data integrity, participants welfare, and protocol compliance.
  • To develop and implement a quality management system for the Repository.
  • To collect and record in the Repository protocol-related clinical information.
  • To organize a consistent system to bank high-quality biospecimens while protecting participant-donor safety and privacy.
  • To establish the policies and procedures for Repository Materials dissemination and research collaboration.
  • To analyze the scientific results of the Repository creation. The secondary aim of the study is to provide a mechanism to store and share for research purposes the de-identified biospecimen and information about participants at risk for adverse pregnancy outcomes.

Conditions

Pregnancy

High-Risk Pregnancy

Study ID

NCT05035160

Start date

Jul 30, 2021

Status verified date

Dec, 2025

Completion date

Dec 31, 2028

Anticipated

Primary completion date

Dec 31, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

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.

Study Design

Enrollment

1000 participants

Anticipated

Interventions and Outcome Measures

Arms

Group 1

Pregnant and postpartum birthing persons with perinatal pathology.

Group 2

Healthy pregnant and postpartum birthing persons.

Group 3

Healthy non-pregnant persons (healthy volunteers).

Primary outcome measure

  • Number of participants of the Perinatal Repository [ Time Frame: From July 30, 2021, to December 31, 2028 ]

Central Contacts and Locations

Central contacts

Locations

Afshar Lab, Department of Obstetrics & Gynecology, UCLA

Recruiting

Los Angeles, California, United States, 90095

Contacts

More Information

Sponsor

Yalda Afshar, MD, PhD

Last update posted

Dec 29, 2025

Last verified

Dec, 2025

Keywords

  • Fetus
  • Obstetrics
  • Perinatal Care
  • Pregnancy
  • Specimen Collection

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-12. This information was provided to ClinicalTrials.gov by Yalda Afshar, MD, PhD on 2025-12-29.