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Clinical Trials/NCT00549237
NCT00549237
Completed
Not Applicable

Perioperative Nutrition in Gastric Bypass Surgery for Morbid Obesity

University Hospital, Geneva1 site in 1 country200 target enrollmentNovember 2007
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ConditionsPostoperative ComplicationsGastric Bypass

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Complications
Sponsor
University Hospital, Geneva
Enrollment
200
Locations
1
Primary Endpoint
Post-operative body mass composition
Status
Completed
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The aim of this study is to demonstrate the influence of peri-operative nutrition on the preservation of lean body mass after gastric bypass, as well as it's influence on postoperative complications.

Detailed Description

Outcome measures: * Lean body mass * Length of hospital stay * Weight loss * Postoperative complications * Cost

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
November 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •RYGBP surgery planned
  • •Age over 18
  • •Informed consent

Exclusion Criteria

  • •Previous bariatric surgery

Outcomes

Primary Outcomes

Post-operative body mass composition

Time Frame: 2 years

Secondary Outcomes

  • Post-operative complications(30 days)
  • Length of stay(2 weeks)

Study Sites (1)

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