A clinical trial to study the effect of epidural bupivacaine(local anaesthetic)by interval drug dosing and by patient controlled Analgesia with Epidural Bupivacaine(local anaesthetic)for pain control.
Phase 2
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/066605
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age:18-60 years
All patients of lower limb surgeries.
All patients having major abdominal surgeries and thoracotomy.
Patients giving consent for procedure.
Exclusion Criteria
Patients with Hypotension, Cardiogenic and Spinal Shock
Patients with Septicemia.
Mechanically ventilated patients.
Patient having coagulopathy/ on anticoagulants /bleeding.
Patient with History of head trauma.
known allergic to any local anesthetic.
Unconcious patient.
Refused to give consent for Epidural placement.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare pain intensityTimepoint: 1st hour and 48 hours
- Secondary Outcome Measures
Name Time Method 1.Patient satisfaction <br/ ><br>2.Additional analgesic requirementsTimepoint: 48 hours