Study to compare postoperative pain relief following two different nerve block adductor canal block and femoral nerve block
Not Applicable
- Conditions
- Health Condition 1: M20-M25- Other joint disorders
- Registration Number
- CTRI/2020/07/026399
- Lead Sponsor
- Azeezia Medical Collage
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of ASA physical status 1-2, aged between 18-80 years, undergoing knee surgery
Exclusion Criteria
Patients with
1) History of chronic pain defined as daily or almost daily (most days of a week) use of opioids for >three months
2) History of peripheral neuropathy or neurologic and/ deficits,
3)Infection at the site of injections,
4)Coagulopathies
5)Refusal to the use of peripheral nerve blocks,
6)Contraindications to spinal or epidural anaesthesia
7)H/o of drug allergies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)To compare the efficacy of postoperative pain relief following Subsartorial adductor canal vs femoral nerve block <br/ ><br>2)To evaluate motor strength after knee surgery between Subsartorial adductor canal vs femoral nerve block <br/ ><br>Timepoint: 6,12,18,24 Hours postoperatively
- Secondary Outcome Measures
Name Time Method To assess postoperative sensory recovery following Subsartorial adductor canal vs femoral nerve blockTimepoint: 6,12,18,24 hours postoperatively