The effect of adding magnesium to bupivacaine for femoral nerve block on postoperative pain in patients undergoing knee and femoral orthopedic operations

Phase 2

• Conditions: Condition 1: Postoperative Analgesia. Condition 2: Postoperative Analgesia.; Acute pain; Pain due to orthopedic internal implantation, fixation and other procedure

• Registration Number: IRCT201410137984N19
• Lead Sponsor: Vice chancellor for research, Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

Patients' consent? No usage of anti- coagulant drugs? No infection at the site of injection? Age between 18 and 65 years old? ASA1&2
Exclusion criteria: Patient refusal( no consent of the patients)? Surgery on PCL? Any complication due to injection or drugs, Calcium channel blocker usage, History of advanced renal disease? Allergy to drugs and Central or peripheral neurologic disorders.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: before block-just after block-3-6-12 hours after block. Method of measurement: visual analog scale.

Secondary Outcome Measures

Name	Time	Method
Sedation. Timepoint: Just after block and 3-6-12 hours after block. Method of measurement: Sedation score.;Satisfication. Timepoint: Just after block and 3-6-12 houres after block. Method of measurement: Questionnare.;Additional requirement for opioid analgesics. Timepoint: Just after block and 3-6-12 hours after block. Method of measurement: Total dosage of injected additional analgesic in miligram.