- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01104454
Placenta and Cord Blood Analyses
December 18, 2023 updated by: Arkansas Children's Hospital Research Institute
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Arkansas
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Little Rock, Arkansas, United States, 72202
- Arkansas Children's Nutrition Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Pregnant women who are at least 7 months pregnant
Description
Inclusion Criteria:
- at least 7 months pregnant
- 18 years of age or older
Exclusion Criteria:
- underweight (BMI<18.5)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Placenta, cord blood and umbilical analyses
Time Frame: at delivery
|
at delivery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Aline Andres, Ph.D., University of Arkansas
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2010
Primary Completion (Actual)
January 1, 2012
Study Completion (Actual)
August 7, 2019
Study Registration Dates
First Submitted
April 14, 2010
First Submitted That Met QC Criteria
April 14, 2010
First Posted (Estimated)
April 15, 2010
Study Record Updates
Last Update Posted (Estimated)
December 20, 2023
Last Update Submitted That Met QC Criteria
December 18, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 111576
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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