Body Composition of Infants: Follow-up to Placenta and Cord Blood Analyses

This study has been withdrawn prior to enrollment.

(determined not enough participants would be able to be enrolled and not enough data collected for good analyses)

Sponsor:

ClinicalTrials.gov Identifier:

NCT01464684

First Posted: November 3, 2011

Last Update Posted: April 20, 2017

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.

Information provided by (Responsible Party):

University of Arkansas

Purpose

Investigators will characterize the body composition and metabolism of infants born from lean, overweight or obese mothers from whom they had previously obtained a placenta and/or cord blood as part of the earlier placenta and cord blood study (#111576)

Condition
Infant Body Composition and Metabolism


Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Prospective
Official Title:	Body Composition of Infants: Follow-up to Placenta and Cord Blood Analyses

Further study details as provided by University of Arkansas:

Biospecimen Retention: Samples With DNA

Blood, urine, and a cheek swab may be collected from study participants


Enrollment:	0
Study Start Date:	October 2011
Estimated Study Completion Date:	December 2012
Estimated Primary Completion Date:	December 2012 (Final data collection date for primary outcome measure)

Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:	3 Months to 21 Months (Child)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	Yes
Sampling Method:	Non-Probability Sample

Study Population

infants age 12 months (+/- 9 months)

Criteria

Inclusion Criteria:

mother's prior participation in study #111576 with successful collection of placenta
infant age 12 months (+/- 9 months)

Exclusion Criteria:

mother did not participate in study #111576
mother did participate in study #111576, but collection of placenta was not successful
infant not age 12 months (+/- 9 months)

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01464684

Sponsors and Collaborators

University of Arkansas

Investigators


Principal Investigator:	Aline Andres, PhD	University of Arkansas

More Information


Responsible Party:	University of Arkansas
ClinicalTrials.gov Identifier:	NCT01464684 History of Changes
Other Study ID Numbers:	132624
First Submitted:	October 31, 2011
First Posted:	November 3, 2011
Last Update Posted:	April 20, 2017
Last Verified:	April 2017

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