Placenta and Cord Blood Analyses
This trial is active, not recruiting.
|Sponsor||Arkansas Children's Hospital Research Institute|
|Start date||March 2010|
|End date||January 2012|
|Trial size||60 participants|
|Trial identifier||NCT01104454, 111576|
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.
Placenta, cord blood and umbilical analyses
time frame: at delivery
Female participants at least 18 years old.
Inclusion Criteria: - at least 7 months pregnant - 18 years of age or older Exclusion Criteria: - underweight (BMI<18.5)
|Official title||Placenta and Cord Blood Analyses|
|Principal investigator||Aline Andres, Ph.D.|
Call for more information