Placenta and Cord Blood Analyses
Completed
- Conditions
- Healthy
- Registration Number
- NCT01104454
- Lead Sponsor
- Arkansas Children's Hospital Research Institute
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
- at least 7 months pregnant
- 18 years of age or older
Exclusion Criteria
- underweight (BMI<18.5)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Placenta, cord blood and umbilical analyses at delivery
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular differences in placenta and cord blood samples correlate with maternal obesity in NCT01104454?
How do placental biomarkers from NCT01104454 compare to standard maternal health indicators in predicting neonatal outcomes?
What are the standardized protocols for placenta and cord blood sample processing in the Arkansas Children's Hospital Research Institute trial NCT01104454?
Are there specific metabolic or inflammatory biomarkers in cord blood associated with maternal weight status as identified in NCT01104454?
How does maternal BMI affect placental gene expression profiles according to the NCT01104454 observational study?
Trial Locations
- Locations (1)
Arkansas Children's Nutrition Center
🇺🇸Little Rock, Arkansas, United States
Arkansas Children's Nutrition Center🇺🇸Little Rock, Arkansas, United States