Placenta and Cord Blood Analyses
Sponsor
Arkansas Children's Hospital Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT01104454
Collaborator
(none)
60
1
113.2
0.5
Study Details
Study Description
Brief 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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
60 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Placenta and Cord Blood Analyses
Actual Study Start Date
:
Mar 1, 2010
Actual Primary Completion Date
:
Jan 1, 2012
Actual Study Completion Date
:
Aug 7, 2019
Outcome Measures
Primary Outcome Measures
- Placenta, cord blood and umbilical analyses [at delivery]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
-
at least 7 months pregnant
-
18 years of age or older
Exclusion Criteria:
- underweight (BMI<18.5)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Arkansas Children's Nutrition Center | Little Rock | Arkansas | United States | 72202 |
Sponsors and Collaborators
- Arkansas Children's Hospital Research Institute
Investigators
- Principal Investigator: Aline Andres, Ph.D., University of Arkansas
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Arkansas Children's Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT01104454
Other Study ID Numbers:
- 111576
First Posted:
Apr 15, 2010
Last Update Posted:
Apr 14, 2020
Last Verified:
Apr 1, 2020
Keywords provided by Arkansas Children's Hospital Research Institute