It is a study done in lower limb surgeries to assess postoperative analgesia for 24hours. The study is done to assess and compare the efficacy of epidural magnesium sulphate with and without bupivacaine .
Phase 3
- Conditions
- Health Condition 1: - Health Condition 2: M848- Other disorders of continuity of bone
- Registration Number
- CTRI/2022/10/046448
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.All patients posted for lower limb surgeries
2.Age group 18-60 years
3.Patients of American Society of Anaesthesiology
grade 1 and 2
Exclusion Criteria
1.Patients on any opioid or any sedative
medication in the weak prior to the surgery
2.Patients with history of alcohol or drug abuse
3.Patients who have known allergies to any of test
drugs
4.Patients with coagulation disorders or on
anticoagulant drugs
5.Patients with cardiac disease[heart
block,premature ventricular
contractions,significant bradyarrhythmias,left
ventricular failure]
6.Patients with respiratory distress
7.Containdications to epidural anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method