Clinical Trials Directory

Trials / Completed

CompletedNCT01632215

Preoperative Gabapentine for Carpal Tunnel

Effect of Preoperative Gabapentine for Carpal Tunnel Syndrome

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Federal University of São Paulo · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to evaluate the postoperative analgesic effect of preoperative gabapentine for carpal tunnel syndrome surgery.

Detailed description

There was studied 40 patients. Group 1 patients received 600 mg of gabapentin 1 hour before surgery; G2 received placebo 1 hour before surgery. Anesthesia was regional intravenous block. Postoperative analgesia when needed was with acetaminophen. If needed was administered codeine. The evaluation of neuropathic pain was made by DN4 questionnaire. Pain intensity was assessed by numeric scale at block and after 30min, 1h, 2h, 2wk, 4wk, 6m. It was noted the duration of analgesia, and the amount of acetaminophen and codeine. The statistical program used for analysis of the results was the Instat Graph

Conditions

Interventions

TypeNameDescription
DRUGGabapentineGabapentine 600 mg 01 dose
OTHERSugar pillSugar pill 01 dose

Timeline

Start date
2010-03-01
Primary completion
2011-08-01
Completion
2012-03-01
First posted
2012-07-02
Last updated
2019-03-05
Results posted
2014-06-04

Source: ClinicalTrials.gov record NCT01632215. Inclusion in this directory is not an endorsement.