A clinical trial to compare effect of two nerve blocks PENG block around shoulder and Superior brachial trunk block in decreasing pain after arthroscopic shoulder surgeries.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecifiedHealth Condition 2: 4- Measurement and MonitoringHealth Condition 3: 8- Other Procedures
- Registration Number
- CTRI/2022/04/041990
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) ASA I to III patients.
2) Age group of 18-80
3) Scheduled for elective unilateral arthroscopic
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 anaesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare Cumulative opioid <br/ ><br>consumption at 24hrs, after arthroscopic shoulder surgery <br/ ><br>between superior brachial trunk block and PENG block around shoulder with a prespecified non inferiority level of 15%.Timepoint: 24hrs after surgery.
- Secondary Outcome Measures
Name Time Method To compare between the two groups the following parameters: <br/ ><br>1) 24hr pain intensity on an 11-point numerical rating score <br/ ><br>2) Time for first analgesic requirement <br/ ><br>3) Motor blockade <br/ ><br>4) Patient satisfaction with pain relief at 24hrs <br/ ><br>5) Surgeon Satisfaction <br/ ><br>6) Diaphragmatic Excursion <br/ ><br>7) complicationsTimepoint: During intra operative period and 24hrs postoperatively