Comparing three different volume of injections in providing pain relief for patients undergoing surgeries in arm using ultrasound guidance
Not Applicable
Completed
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2020/12/029528
- Lead Sponsor
- SRM Medical College Hospital and Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
ASA 1 and ASA 2
Weight between 50 to 100kgs
Exclusion Criteria
Pregnancy
Drug allergy
Patient refusal
Uncooperative patients
Coagulation disorders
Pre-existing diaphragmatic paresis
Severe respiratory illnesses (COPD/ILD)
Pre-existing neurological deficit in upper limb
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the incidence of hemi diaphragmatic paresis following Interscalene brachial plexus block (IBPB) performed using three different volumes of local anaestheticsTimepoint: Till 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method 1)Success rate of Interscalene brachial plexus block <br/ ><br>2)Onset of sensory blockade <br/ ><br>3)Duration of postoperative analgesia <br/ ><br>4)Adverse effects of IBPB like hoarseness of voice, Horners� syndrome, vascular puncture, pneumothorax <br/ ><br>Timepoint: 1)To reach a score of 2 within 30 min of Interscalene block <br/ ><br>2)Onset time for a sensory block is the time elapsed between the end of the block procedure and the moment when the pinprick test yielded a score of 2 <br/ ><br>3)24hrs postoperatively <br/ ><br>4)Till 24hrs postoperatively <br/ ><br>