Comparison of Analgesic efficacy of continuous adductor canal block with and without IPACK block for postoperative analgesia in patients undergoing total knee replacement.
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/01/049329
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
ASA physical status 1-2
Age 16-65
BMI 18-30 kg/m2
Unilateral Total Knee Replacement for osteoarthritis
Exclusion Criteria
Patient refusing to give informed consent.
History of relevant drug allergy
History of psychiatric illness, substance abuse
Severe cardiovascular, respiratory , metabolic or neurological disease
Pregnancy and lactation
Cogaulopathy
Infection at planned injection site
Patient on steroids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method