Perioperative Nutrition in Gastric Bypass Surgery
The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2010 by University Hospital, Geneva.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
University Hospital, Geneva
Information provided by:
University Hospital, Geneva
ClinicalTrials.gov Identifier:
NCT00549237
First received: October 24, 2007
Last updated: January 14, 2010
Last verified: January 2010
| Tracking Information | |||||||||
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| First Received Date ICMJE | October 24, 2007 | ||||||||
| Last Updated Date | January 14, 2010 | ||||||||
| Start Date ICMJE | November 2007 | ||||||||
| Estimated Primary Completion Date | August 2010 (final data collection date for primary outcome measure) | ||||||||
| Current Primary Outcome Measures ICMJE |
Post-operative body mass composition [ Time Frame: 2 years ] [ Designated as safety issue: No ] | ||||||||
| Original Primary Outcome Measures ICMJE |
Post operative body mass composition [ Time Frame: 2 years ] | ||||||||
| Change History | Complete list of historical versions of study NCT00549237 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Current Other Outcome Measures ICMJE | Not Provided | ||||||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||||||
| Descriptive Information | |||||||||
| Brief Title ICMJE | Perioperative Nutrition in Gastric Bypass Surgery | ||||||||
| Official Title ICMJE | Perioperative Nutrition in Gastric Bypass Surgery for Morbid Obesity | ||||||||
| 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. |
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| Detailed Description | Outcome measures:
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| Study Type ICMJE | Interventional | ||||||||
| Study Phase | Not Provided | ||||||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE |
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| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status ICMJE | Recruiting | ||||||||
| Estimated Enrollment ICMJE | 190 | ||||||||
| Estimated Completion Date | November 2010 | ||||||||
| Estimated Primary Completion Date | August 2010 (final data collection date for primary outcome measure) | ||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | 18 Years and older | ||||||||
| Accepts Healthy Volunteers | No | ||||||||
| Contacts ICMJE |
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| Location Countries ICMJE | Switzerland | ||||||||
| Administrative Information | |||||||||
| NCT Number ICMJE | NCT00549237 | ||||||||
| Other Study ID Numbers ICMJE | CER 07 - 096 | ||||||||
| Has Data Monitoring Committee | No | ||||||||
| Responsible Party | Principal investigator, University Hospital, Geneva | ||||||||
| Study Sponsor ICMJE | University Hospital, Geneva | ||||||||
| Collaborators ICMJE | Not Provided | ||||||||
| Investigators ICMJE |
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| Information Provided By | University Hospital, Geneva | ||||||||
| Verification Date | January 2010 | ||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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