Comparison of onset, duration and quality of supraclavicular block using 0.5% bupivacaine with magnesium sulphate , ketamine and neostigmine in forearm orthopedic surgery

Phase 3

Recruiting

• Conditions: Forearm orthopedic surgery.; Unspecified fracture of forearm; S52.9

• Registration Number: IRCT20141209020258N158
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 May 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

20 -70 years
Candidate for upper limb orthopedic surgery
No more than one fracture in the body or surgery
No blood coagulation diseases and disorders in PTT, PT and INR
Body mass index less than 35
Lack of psychological problems
No pregnant
Absence of neurological disorders in the hand
No allergies to drugs used
Absence of chronic pain syndrome

Exclusion Criteria

Lack of patient cooperation to perform the block
Block failure
Surgery time less than 50 and more than 150 minutes
Need for more sedation than stated in the plan

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: In recovery and 2 ,4, 8, 12 and 24 hours after surgery. Method of measurement: Visual analog scale of pain.;Narcotics consumption. Timepoint: 24 hours after surgery. Method of measurement: Observation.;Sensory block. Timepoint: Every 1 minute. Method of measurement: chronometer.;Motor block. Timepoint: Every 5 minute. Method of measurement: chronometer.