clinical trial to compare two abdominal wall blocks for post operative analgesia in unilateral inguinal hernia repair
Phase 4
- Conditions
- Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2022/04/042176
- Lead Sponsor
- Dr Priyanka Dwivedi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients aged 18 - 60 years old, of either sex, American Society of Anesthesiologists physical status (ASA) I and II, who are scheduled for unilateral inguinal hernia repair under spinal anaesthesia
Exclusion Criteria
Patientââ?¬•s refusal,
Allergies to local anesthetic drugs
Body mass index (BMI) >35 Kg/m
Significant cardiovascular disease, hepatic dysfunction or renal dysfunction, coagulation abnormalities
Infection in the intended intervention site,
Bilateral inguinal hernia or obstructed inguinal hernia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method