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Energy Expenditure and Gastric Bypass Surgery
This study is not yet open for participant recruitment.
Verified by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), March 2009
First Received: March 17, 2009   No Changes Posted
Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier: NCT00863993
  Purpose

The aim of this study is to assess whether activity thermogenesis increases in patients undergoing bariatric surgery post-operatively compared to pre-operatively. The investigators will assess non-exercise activity thermogenesis using a validated Physical Activity Monitoring System and doubly labeled water, immediately pre-operatively and again at 6 and 18 months post-operatively. PAMS has been validated in lean and obese individuals. This is to assess energy expenditure, activity thermogenesis and NEAT during the phase of greatest weight loss and once weight loss has plateaued. This will permit us to address our primary hypothesis that activity thermogenesis as a fraction of total daily energy expenditure increases in patients undergoing bariatric surgery 6 and 18 months post-operatively, compared to pre-operatively.


Condition
Gastric Bypass Surgery

MedlinePlus related topics: Surgery
U.S. FDA Resources
Study Type: Observational
Official Title: Energy Expenditure and Gastric Bypass Surgery
  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

40 healthy patients (M=F, aged 18-60 years) undergoing gastric bypass bariatric surgery will be recruited.

Criteria

Inclusion Criteria:

  • Undergoing gastric bypass surgery, 18-60 years

Exclusion Criteria:

  • Eligible subjects will be excluded who cannot walk at 2.4 mph for 15 minutes, or weigh greater than 227 kg at the screening visit.
  Contacts and Locations
No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Mayo Clinic ( Professor James A Levine )
Study ID Numbers: DK72479
Study First Received: March 17, 2009
Last Updated: March 17, 2009
ClinicalTrials.gov Identifier: NCT00863993     History of Changes
Health Authority: United States: Federal Government

ClinicalTrials.gov processed this record on May 07, 2009