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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
Results First Received: July 21, 2009  
Study Type: Observational
Study Design: Observational Model: Cohort;   Time Perspective: Prospective
Condition: Obesity

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
All Infants One group comprised all infants evaluated.

Participant Flow:   Overall Study
    All Infants  
STARTED     47  
COMPLETED     47  
NOT COMPLETED     0  



  Baseline Characteristics
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Reporting Groups
  Description
Infants No text entered.

Baseline Measures
    Infants  
Number of Participants  
[units: participants]
 		  47  
Age  
[units: participants]
 		 
<=18 years     47  
Between 18 and 65 years     0  
>=65 years     0  
Gender  
[units: participants]
 		 
Female     28  
Male     19  



  Outcome Measures
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1.  Primary:   Infant Adiposity at 24-72 Hours Following Birth   [ Time Frame: 24-72 hours following birth ]
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2.  Primary:   Fetal Abdominal Circumference   [ Time Frame: 35 weeks gestation ]
  Show Outcome Measure 2

3.  Primary:   Estimated Fetal Weight Percentile   [ Time Frame: 35 weeks gestation ]
  Show Outcome Measure 3


  Serious Adverse Events
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  Other Adverse Events
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  More Information
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Certain Agreements:  
All Principal Investigators ARE employed by the organization sponsoring the study.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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Results Point of Contact:  
Name/Title: Laurie Moyer-Mileur
Organization: University of Utah
phone: 801/587-7488
e-mail: Laurie.Moyer-Mileur@hsc.utah.edu


No publications provided


Responsible Party: Laurie Moyer-Mileur, University of Utah
ClinicalTrials.gov Identifier: NCT00715754     History of Changes
Other Study ID Numbers: 18858
Study First Received: July 10, 2008
Results First Received: July 21, 2009
Last Updated: November 24, 2009
Health Authority: United States: Institutional Review Board