Two very low doses of naloxone in combination with ropivacaine on the onset ,severity and duration of axillary block

Phase 3

Recruiting

• Conditions: hand and forearm surgery.; Injuries to the elbow and forearm; S50-S59

• Registration Number: IRCT20170105031787N6
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Candidate patients for hand and forearm surgery
Age between 18-70 years

Exclusion Criteria

Anemia
Sensitivity to local anesthetic drugs
Congenital and acquired neuromuscular diseases
History of seizures
Drug addiction
Heart diseases
Any digestive system disorders.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: Upon entering recovery. Method of measurement: Based on NRS scale.;The amount of drug use. Timepoint: In the first 24 hours after the surgery. Method of measurement: Based on the information in the patient's file.

Secondary Outcome Measures

Name	Time	Method
Duration of numbness. Timepoint: During surgery. Method of measurement: Based on the information in the patient's file.;The first time to ask for drugs. Timepoint: During surgery. Method of measurement: Based on the information in the patient's file.;Ramsy sedation scale. Timepoint: During surgery and upon entering recovery. Method of measurement: Based on the information in the patient's file.;Patient's satisfaction. Timepoint: After surgery. Method of measurement: Based on the Likert scale.