Comparision between two drugs in postoperative pain management in a block used for below knee surgeries.
Not Applicable
- Conditions
- Health Condition 1: M998- Other biomechanical lesions
- Registration Number
- CTRI/2024/03/064144
- Lead Sponsor
- Mysore Medical College and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients of ASA I and II, belonging to age groups 18-65 years, undergoing elective below knee surgery under spinal anesthesia.
Exclusion Criteria
Patient refusal.
ASA grade III and IV.
Drug allergy.
Deranged coagulation profile.
Neurologic or neuromuscular diseases.
Skin infections at the site of injection.
Pregnant and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative analgesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Adverse effectsTimepoint: 24 hours