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Placenta and Cord Blood Analyses

NCT01104454 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2023-12-20

No results posted yet for this study

Summary

The purpose of this study is to standardize methods in collecting and processing placenta, umbilical cord and cord blood samples. Samples will be used to determine potential differences between normal weight, overweight and obese individuals.

Conditions

  • Healthy

Sponsors & Collaborators

  • Arkansas Children's Hospital Research Institute

    lead OTHER

Principal Investigators

  • Aline Andres, Ph.D. · University of Arkansas

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2012-01-31
Completion
2019-08-07

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01104454 on ClinicalTrials.gov