To compare effect of two different nerve blocks in unilateral total knee replacement
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: 8- Other Procedures
- Registration Number
- CTRI/2024/03/063773
- Lead Sponsor
- Josemine Davis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Adults aged 18 years and older undergoing unilateral TKR
2.ASA classification I-III.
3.Patients capable of providing informed consent or with consent provided by a legal guardian.
4.Patients who can comprehend and cooperate with study procedures and pain assessment tools.
1.Patients with contraindications or allergies to local anaesthetics used in nerve block procedures.
2.Patients scheduled for emergency orthopaedic procedures.
3.Patients with chronic opioid use or opioid tolerance.
4.Patients with pre-existing neurological disorders that may affect pain perception.
5.Patients with coagulopathies or those on anticoagulant therapy that cannot be temporarily stopped.
6.Known allergies to components of the nerve block procedures.
7.Patients with active infections or open wounds at the site of the nerve block.
8.Pregnant or lactating women.
9.Patients currently enrolled in other clinical trials or studies involving pain management techniques.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Evaluate Postoperative Pain ReliefTimepoint: At baseline , 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method To examine functional outcomes: Assess the impact of the AFCNB & ACB on early ambulation & functional recovery in the immediate postoperative period. The Timed Up & Go (TUG) test results at 24 hours postoperatively will be noted in comparison to pre-op TUG test results.Timepoint: 24 hours