Evaluation of analgesic effect of lidocaine on forearm anesthesia in carpal tunnel syndrome surgery

Not Applicable

Recruiting

• Conditions: G56.00; Carpal tunnel syndrome, unspecified upper limb.; Carpal tunnel syndrome, unspecified upper limb

• Registration Number: IRCT20160926029976N6
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 August 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

All patients with carpal tunnel syndrome candidate for surgery

Exclusion Criteria

Emergency operation
Class ASA ?,?
Sensitivity to NSAIDs
Psychological disorders
Heart failure
Renal failure
Liver failure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Onset of pain after opening the tourniquet. Timepoint: Measure of onset of pain 1 and 24 hours after opening the tourniquet. Method of measurement: Hour.;Quality of analgesia. Timepoint: Measure of Quality of analgesia 1 and 24 hours after opening the tourniquet. Method of measurement: visual analogue scale.;The amount of received analgesic. Timepoint: Measuring the amount of received analgesic within surgery and 1, 24 hours after surgery. Method of measurement: Dosage (mg).;Changes in blood pressure. Timepoint: Recording of changes in blood pressure within surgery and 1, 24 hours after surgery. Method of measurement: Sphygmomanometer.