Comparison of onset and duration of pain prescribed by combination of bupivacaine with 5% dextrose and fentanyl with bupivacaine

Phase 3

Recruiting

• Conditions: Fracture of shaft of tibia.; Fracture of shaft of tibia; S82.2

• Registration Number: IRCT20190618043934N2
• Lead Sponsor: Birjand University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Having conscious patient satisfaction
Patients with ASA class one and two
Age between 20 and 50 years
No drug addiction
No spinal history following surgery in the past week
No pregnancy
Nhere is no spinal deformity
There is no spinal deformity

Exclusion Criteria

Patient dissatisfaction to continue studying
Duration of surgery over 1 hour
Inability to position the patient
Spinal Infection
Sensitivity to local Anesthetic Drugs
High ICP
Coagulation Disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: 0, 6, 12and 24 hours after surgery. Method of measurement: Using of VAS.