Magnesium Sulphate for postoperative pain management

Not Applicable

• Conditions: Surgery; Postoperative Pain

• Registration Number: PACTR201503001053196
• Lead Sponsor: Cairo University Hospitals

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-03-03
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

ASA physical status I and II
aging from 18 to 60 years
scheduled for arthroscopic ACL reconstruction

Exclusion Criteria

Patients with hepatic, renal, cardiac, hematological, or respiratory impairment, diabetic patients,
morbidly obese,
pregnant,
patients with history of neuropathy, myopathy and neuromuscular diseases, patients with prior treatment with corticosteroids, calcium channel blockers, opioids
patients with cognitive dysfunction that may interfere with the patient ability to provide reliable information about their postoperative pain

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
intensity of postoperative pain at rest as assessed by 0-10 visual analogue pain score (VAS).

Secondary Outcome Measures

Name	Time	Method
Dynamic visual analogue pain score with movement (knee flexion).;The period of bearable pain;The total postoperative analgesic doses of diclofenac and the number of pethidine rescue doses;Side-effects;Serum magnesium levels