comparing two different blocks for pain relief after total knee replacement
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/050438
- Lead Sponsor
- Sree Balaji medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA 1,2,3
2.Patients posted for total knee arthroplasty
Exclusion Criteria
1. ASA 4 Patients
2. Patients with Neurological disorders.
3. Bleeding disorder
4. Infection or Sepsis
5. Patients with local anesthetics allergy
6 Not willing to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. NRS pain score <br/ ><br>2.Duration of analgesiaTimepoint: 1. pain score assessed every 4th hour from 4th to 48th hour postoperatively <br/ ><br>2. Duration 0f analgesia marked by administration of rescue analgesia when NRS pain score is more than 3.
- Secondary Outcome Measures
Name Time Method 1.Total opioid consumption <br/ ><br>2.Early ambulation <br/ ><br>3.Adverse events-pain or paraesthesia in the thigh, or features of local anaesthetic toxicityTimepoint: 1.Total opioid consumption over first 24 hour <br/ ><br>2.Early ambulation assessed by TUG(Timed Up and Go test) and SLR test at 24 th hour postoperatively. <br/ ><br>3.Will be noted if any.