to compare the effect of two nerve blocks on postoperative pain relief
Not Applicable
- Conditions
- Health Condition 1: M259- Joint disorder, unspecified
- Registration Number
- CTRI/2022/04/042293
- Lead Sponsor
- Sancheti Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Scheduled for elective unilateral arthroscopic shoulder surgery.
Exclusion Criteria
1. Patients who refused to participate in the study.
2. Patients with a history of cardiac, renal, or hepatic disease.
3. Patients with pre-existing neurologic deficits or neuropathy affecting the brachial plexus.
4. Patients with contraindications to peripheral nerve block.
5. Patients with known allergy to local anaesthetic drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method