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Clinical Trials/NCT00532896
NCT00532896
Completed
Not Applicable

Impact of Weight Loss Following Bariatric Surgery on Pulmonary Function in Patients With Morbid Obesity

Laval University1 site in 1 country60 target enrollmentApril 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bariatric Surgery
Sponsor
Laval University
Enrollment
60
Locations
1
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Increase in body mass index (BMI)is associated with a decrease in expiratory flows.Obesity is also associated with an increased prevalence of asthma.Consequences of obesity on respiratory function and on bronchial responsiveness are still to be documented.

This study aims to evaluate, before and after surgery, the impact of a bariatric surgery (biliopancreatic diversion with duodenal switch)on respiratory function in patients with morbid obesity .

Our hypothesis is that weight loss following bariatric surgery will induce significant improvements in pulmonary function and airway responsiveness, and, as a consequence, a reduction in respiratory symptoms,these changes being correlated with a reduction in systemic markers of inflammation. Maintenance of weight loss after one year will permit the persistence of these improvements

Detailed Description

Patients will be evaluated before the surgery (time zero), 6 months and one year after their surgery. A control group of patients on a waiting list for bariatric surgery will be evaluated at time zero and after 6 months and one year. At each visit,patients will: * fill a standardized respiratory questionnaire and a questionnaire on sleep apnea; questionnaires on asthma control will be completed by patients with asthma. * have a spirometry, pulmonary volumes measures by body plethysmography and methacholine inhalation test with evaluation of symptoms perception. * an induced sputum will be performed. * A blood sample will be drawn to evaluate inflammation and measure C-reactive protein concentration in plasma. * An allergy skin prick test will be done at time zero.

Registry
clinicaltrials.gov
Start Date
April 2006
End Date
May 2011
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Louis-Philippe Boulet

MD, FRCPC, FCCP

Laval University

Eligibility Criteria

Inclusion Criteria

  • Body mass index \>or= 35 kg/m2
  • Non-smokers or ex-smokers (\<10 packs-year)

Exclusion Criteria

  • Previous bariatric surgery
  • previous vagotomy
  • no compliance to visits
  • subjects unable to provide an informed consent or to understand the questions included in questionnaires
  • Patients with cardiac pacemaker
  • hemodynamically significant valvulopathy

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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