Placenta and Cord Blood Analyses

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01104454

Enrollment

Registered

2010-04-15

Start date

2010-03-31

Completion date

2019-08-07

Last updated

2023-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

healthy pregnant women

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* at least 7 months pregnant * 18 years of age or older

Exclusion criteria

* underweight (BMI\<18.5)

Design outcomes

Primary

Measure	Time frame
Placenta, cord blood and umbilical analyses	at delivery

Countries

United States

Outcome results