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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01104454
Other study ID # 111576
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2010
Est. completion date August 7, 2019

Study information

Verified date December 2023
Source Arkansas Children's Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 7, 2019
Est. primary completion date January 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - at least 7 months pregnant - 18 years of age or older Exclusion Criteria: - underweight (BMI<18.5)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Arkansas Children's Nutrition Center Little Rock Arkansas

Sponsors (1)

Lead Sponsor Collaborator
Arkansas Children's Hospital Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Placenta, cord blood and umbilical analyses at delivery
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