A clinical trial to study the effects of two drugs, Ropivacaine and Levobupivacaine in patients undergoing surgery in Epidural anaesthesia.
Phase 4
Completed
- Conditions
- Health Condition 1: null- Epidural Anaesthesia for lower abdominal surgery
- Registration Number
- CTRI/2016/10/007341
- Lead Sponsor
- Dr Aditi Suri
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Patients with ASA Grade I and II
Exclusion Criteria
•Patient refusal.
•Contraindications to epidural.
Pre-existing neurological deficits in the lower extremities, and
Cardiorespiratory diseases,
neurological or psychological disease,
hepatic, or renal disease.
Bleeding diathesis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method SENSORY <br/ ><br>1.Onset <br/ ><br>2.Duration <br/ ><br>3.Highest level <br/ ><br> <br/ ><br>MOTOR <br/ ><br>1.Onset <br/ ><br>2.Duration <br/ ><br>Timepoint: SENSORY <br/ ><br>1.Onset: time till T10 level attained. <br/ ><br>2.Duration: time till two segment regression. <br/ ><br>3.Highest level of sensory block achieved. <br/ ><br> <br/ ><br>MOTOR <br/ ><br>1.Onset: Bromage scale III block. <br/ ><br>2.Duration: Bromage scale score 0.
- Secondary Outcome Measures
Name Time Method postoperative analgesia and haemodynamic changesTimepoint: duration of post operative analgesia 3.5-4hrs