compare effect of two nerve blocks for pain relief in shoulder manipulatio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057680
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA I to III patients.
2. Age group of 18-70 years.
3. Scheduled for elective unilateral shoulder manipulation procedure.
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 To compare total postoperative morphine consumption in 24hrs between patients undergoing ISB and PENG block around shoulder for shoulder manipulation surgeryTimepoint: 24hrs after block
- Secondary Outcome Measures
Name Time Method • Successful completion of manipulation procedure <br/ ><br>•Ease of procedure on a Likert Scale of 0-2 <br/ ><br>•Visual analogue scale (VAS) score for pain ranging from 0 - 10 <br/ ><br>•Pre & post- block Diaphragmatic excursion <br/ ><br>•Incidence of motor block (0, 8, 24 hr) <br/ ><br>•Proportion of patients with moderate to severe pain (VAS more than 4) <br/ ><br>• Motor blockade after block (total/partial/absent) <br/ ><br>•Time for initiation of shoulder mobilisation <br/ ><br>•Degree of Shoulder abduction possible at 24 hrs <br/ ><br>•Patient satisfaction (0-10) at 24 hrs postoperatively ( vascular puncture, parasthesia, LA toxicity, hoarsness, PONV) <br/ ><br>Timepoint: time point 0,2,4, 8 and 24 hours after the procedure