Pain after two different multimodal anesthesia techniques in obesity surgery

Not Applicable

• Conditions: Obesity; Acute postoperative pain; Y en Roux Gastroplasty; R52.0; E02.570.500.062.750

• Registration Number: RBR-9ftypy
• Lead Sponsor: Santa Casa de Misericórida de Belo Horizonte

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-08-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients sequentially scheduled for Roux-en-Y Reduction Gastroplasty; age between 18 and 70 years; agreement and signature of the free and informed consent term.

Exclusion Criteria

Chronic use of opioids; patients with chronic pain; history of chemical dependence; allergic to any of the medications used in the study; patients with any cardiac, respiratory, renal or hepatic pathology that is considered severe.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome expected: Reduction of postoperative pain in the group 2 DEX-FENTA compared to the REMI group, evaluated by the 11-point verbal pain scale (0 to 10). Evaluations performed after 1, 4 and 24 hours after the surgery.;Primary outcome observed: During the first hour after the procedure patients in Group 2 DEX-FENTA showed a lower pain score in comparison with those in Group 1 REMI (p<0.05). Pain scale score evaluations 4 and 24 hours after the procedure were similar in both groups.