Comparison of the success rate of combined block in arm surgeries

Phase 3

Recruiting

• Conditions: ocal anesthesia to the arm, forearm and hand.; Other complications of procedures, not elsewhere classified; T81.8

• Registration Number: IRCT20211017052786N3
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Patients with American Stroke Association (ASA) 1, 2
Patients with arm fractures require surgery
Patients over 18 years of age

Exclusion Criteria

Drug addiction
Patient dissatisfaction
Being pregnant
has a history of allergy to local anesthetics

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain medication required. Timepoint: 6 and 12 hours after surgery. Method of measurement: Visual analog scale.