A RANDOMISED DOUBLE BLIND CONTROL STUDY TO COMPARE THE EFFICACY OF TWO DIFFERENT STRENGTH OF BUPRENOPHINE AS A SPINAL ADJUVANT WITH 0.75% ROPIVACAINE IN ADULT PATIENT UNDERGOING OPEN INGUINAL HERNIA SURGERIES.
Not Applicable
- Conditions
- Health Condition 1: K400- Bilateral inguinal hernia, with obstruction, without gangrene
- Registration Number
- CTRI/2023/12/060726
- Lead Sponsor
- MGIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
?American Society of Anesthesiologists Grade I and II patients.
?Age above 18 years of any gender
?Patients undergoing open Inguinal hernia Surgeries.
?Height is more than 4 feet.
Exclusion Criteria
?American Society of Anesthesiologists Grade III and IV patients.
?Patients with known contraindications for spinal anaesthesia: bleeding disorders, local infection.
?Patients with hemodynamic instability.
?Patient with allergy to or history of hypersensitivity to local anaesthetic.
?Emergency surgeries.
?Patient’s refusal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method