Antecedents of Obesity: Fetal Measures of Adiposity (FEMA)

This study has been completed.

Sponsor:

Information provided by:

University of Utah

ClinicalTrials.gov Identifier:

NCT00715754

First received: July 10, 2008

Last updated: November 24, 2009

Last verified: November 2009

History of Changes

Tracking Information

First Received Date ^ICMJE

July 10, 2008

Last Updated Date

November 24, 2009

Start Date ^ICMJE

September 2006

Primary Completion Date

February 2009 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

Infant Adiposity at 24-72 Hours Following Birth [ Time Frame: 24-72 hours following birth ] [ Designated as safety issue: No ]
Fetal Abdominal Circumference [ Time Frame: 35 weeks gestation ] [ Designated as safety issue: No ]
Estimated Fetal Weight Percentile [ Time Frame: 35 weeks gestation ] [ Designated as safety issue: No ]

Original Primary Outcome Measures ^ICMJE

Not Provided

Change History

Complete list of historical versions of study NCT00715754 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Not Provided

Original Secondary Outcome Measures ^ICMJE

Not Provided

Current Other Outcome Measures ^ICMJE

Not Provided

Original Other Outcome Measures ^ICMJE

Not Provided

Descriptive Information

Brief Title ^ICMJE

Antecedents of Obesity: Fetal Measures of Adiposity

Official Title ^ICMJE

Antecedents of Obesity: Fetal Measures of Adiposity, "A Plan for Obesity Disaster Management"

Brief Summary

The purpose of this research is to study whether fetal biometrics obtained by 2-D ultrasound can predict infant adiposity by air displacement plethysmography at birth.

Detailed Description

Not Provided

Study Type ^ICMJE

Observational

Study Design ^ICMJE

Observational Model: Cohort
Time Perspective: Prospective

Target Follow-Up Duration

Not Provided

Biospecimen

Not Provided

Sampling Method

Non-Probability Sample

Study Population

Children born at the University of Utah Hospital, whose mothers received prenatal care also at the University of Utah Hospital.

Condition ^ICMJE

Obesity

Intervention ^ICMJE

Not Provided

Study Group/Cohort (s)

Not Provided

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Enrollment ^ICMJE

Completion Date

February 2009

Primary Completion Date

February 2009 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

Infants of mothers between the ages of 18 and 45, planning child birth at the University of Utah Hospital, and willing to provide parental permission for the child to participate in the study.

Exclusion Criteria:

Infants of mothers under the age of 18, over the age of 45, planning child birth at another facility other than the University of Utah Hospital, or who are not willing to provide permission for the child to participate in the study.

Gender

Both

Ages

up to 72 Hours

Accepts Healthy Volunteers

Yes

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

United States

Administrative Information

NCT Number ^ICMJE

NCT00715754

Other Study ID Numbers ^ICMJE

18858

Has Data Monitoring Committee

Responsible Party

Laurie Moyer-Mileur, University of Utah

Study Sponsor ^ICMJE

University of Utah

Collaborators ^ICMJE

Not Provided

Investigators ^ICMJE

Principal Investigator:

Laurie Moyer-Mileur, PhD

University of Utah

Information Provided By

University of Utah

Verification Date

November 2009

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top