Dexmedetomidine and Fentanyl are compared being an adjuvant to Levobupivacaine in case of upper limb surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/069905
- Lead Sponsor
- Peoples College of Medical Sciences And Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade 1 and 2
All patients scheduled for elective upper limb surgeries under Supraclavicular Brachial Plexus Block
Exclusion Criteria
Patient not giving consent
Age less than 18 years and more than 60years
ASA grade 3 and more
Patients with abnormal coagulation profile
Patient with history of opioid abuse
Patients with local skin site infections
Patients with hypersensitivity to any of the drugs used
Pregnant and lactating mothers
Failure of Block
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of sensory and motor blockade in the form of response to pin prick test and modified bromage scaleTimepoint: 300 minutes or the entire duration of surgery whichever is earlier
- Secondary Outcome Measures
Name Time Method Onset of sensory & motor blockadeTimepoint: For approximately 60 minutes after the administration of the drug