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Clinical Trials/NCT01321983
NCT01321983
Completed
Not Applicable

Effects of Preoperative Inspiratory Muscle Training (IMT) in Obese Women Undergoing Open Bariatric Surgery: Respiratory Muscle Strength, Lung Volumes and Diaphragmatic Excursion

Universidade Federal de Sao Carlos1 site in 1 countryMarch 24, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Preoperative Inspiratory Muscular Training
Sponsor
Universidade Federal de Sao Carlos
Locations
1
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

OBJECTIVE: to determine whether preoperative inspiratory muscle training (IMT) is able to attenuate the impact of surgical trauma on the respiratory muscle strength, in the lung volumes and diaphragmatic excursion in obese women undergoing open bariatric surgery.

Therefore, the hypothesis of the present study was that preoperative IMT is able to attenuate the negative effects of surgical trauma on the respiratory muscle strength, in the lung volumes and diaphragmatic excursion, thus reducing the risk of PPC, in obese patients undergoing open bariatric surgery.

DESIGN: Randomized controlled trial. SETTING: Meridional Hospital, Cariacica/ES, Brazil. SUBJECTS: Thirty-two obese women undergoing elective open bariatric surgery were randomly assigned to receive preoperative inspiratory muscle training (IMT group) or usual care (control group).

MAIN MEASURES: Respiratory muscle strength (maximal inspiratory pressure - MIP and maximal expiratory pressure - MEP), lung volumes and diaphragmatic excursion.

Registry
clinicaltrials.gov
Start Date
March 24, 2011
End Date
TBD
Last Updated
15 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Universidade Federal de Sao Carlos

Eligibility Criteria

Inclusion Criteria

  • Over 18 years of age,
  • No smoking or respiratory disease.

Exclusion Criteria

  • Patients who refused to participate in the steps of the research protocol,
  • Patients with a history of prior abdominal surgery,
  • Patients who were unable to understand and perform the tests properly
  • Patients who refused to sign the Informed Consent Term.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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