Study to compare dexamethasone and dexmeditomidine as additive with local anaesthetic in shoulder surgeries.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/067288
- Lead Sponsor
- Shri B M Patil Medical College Hospital and Research Centre Vijayapur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients admitted for shoulder surgeries under interscalene brachial plexus block with ASA grade I and II
Exclusion Criteria
1. Infection at the site of injection.
2. Known allergy/hypersensitivity to local anaesthetic drug.
3. presence of coagulopathies.
4. A history of cardiac, respiratory, hepatic and renal failure and those who refused local amaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Assess onset and duration of sensory block. <br/ ><br>2. Assess onset and duration of motor block. <br/ ><br>3. To evaluate additive effects of dexamethasone and dexmeditomidine to levobupivacaineTimepoint: baseline
- Secondary Outcome Measures
Name Time Method Assessment of post operative visual analogue scores for both groups at 2, 6, 8, 10, & 12 hours after surgery, patient satisfaction score at 24hTimepoint: 24 hours;To monitor intraoperative hemodynamic stability.Timepoint: baseline;To study ISBPB related post operative complications.Timepoint: 24 hours;To study the time taken for first rescue analgesia & requirement of total dose of rescue analgesia.Timepoint: 24 hours