Status:
COMPLETED
Intraoperative Fluid Management in Laparoscopic Bariatric Surgery
Lead Sponsor:
Tel-Aviv Sourasky Medical Center
Conditions:
Morbid Obesity
Acidosis
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The objective of this study is to evaluate the effects of 'high' versus 'low' volume intraoperative fluid administration (Ringer Lactate, RL) on intra- and postoperative parameters, in obese patients ...
Detailed Description
Obesity, a chronic disease that is increasing in prevalence in adults, adolescents, and children, is now considered to be a global epidemic. The prevalence of obesity has increased markedly in the las...
Eligibility Criteria
Inclusion
- Adult patients ( \>18 years) with an American Society of Anesthesiology physical status of I-III who were presenting for laparoscopic bariatric surgery, were prospectively studied.
- Patients were considered eligible if they had a BMI \> 40, or \> 35 and at least one comorbid condition and were scheduled to undergo one of the following laparoscopic operations:
- Roux-Y Gastric Bypass (LRYGB)
- Biliopancreatic Diversion with Duodenal Switch (LDS), or
- Sleeve Gastrectomy (LSG).
Exclusion
- Patients aged younger than 18 years.
- Patients with renal dysfunction (creatinine \> 50% upper limit of normal value).
- Congestive heart failure.
Key Trial Info
Start Date :
April 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2008
Estimated Enrollment :
107 Patients enrolled
Trial Details
Trial ID
NCT00905502
Start Date
April 1 2007
End Date
December 1 2008
Last Update
May 20 2009
Active Locations (1)
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1
Hadassah Medical Organization
Jerusalem, Israel, 91120