comparison of effects with dexmedetomidine and dexamethasone as an adjuvant to bupivacaine in supraclavicular block in adult patients undergoing forearm and hand surgeries
Phase 4
- Conditions
- Health Condition 1: T23- Burn and corrosion of wrist and handHealth Condition 2: S62- Fracture at wrist and hand levelHealth Condition 3: S52- Fracture of forearmHealth Condition 4: O- Medical and SurgicalHealth Condition 5: T79A- Traumatic compartment syndrome
- Registration Number
- CTRI/2021/04/032594
- Lead Sponsor
- VMMC Safdarjung hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiologists grade l and ll patients undergoing forearm and hand surgeries
Exclusion Criteria
Known allergy to study drugs,pregnancy and lactation,patients with pre-existing peripheral neuropathy and coagulation disorders,infection at site of injection,patients on beta blockers and anti-hypertensive therapy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method onset and duration of sensory and motor block when dexmedetomidine or dexamethasone are used as an adjuvant to bupivacaine in supraclavicular brachial plexus block in adult patients undergoing forearm and hand surgeriesTimepoint: onset of sensory and motor block will be assessed once in every minute <br/ ><br>duration of sensory and motor block will be assessed once in an hour
- Secondary Outcome Measures
Name Time Method intraoperative hemodynamic changesTimepoint: 5mins,10mins,15mins,30mins,45mins,1hour,1hour 30mins,2hours,2hour s30mins,3hours;time to first rescue analgesiaTimepoint: hourly assessment