CTRI/2020/09/027929Not yet recruitingNot Applicable
Comparative evaluation of analgesic efficacy of different dose of Dexamethasone as adjuvant to Levobupivacaine in ultrasound guided brachial plexus block in upper limb surgeries.
Department of Anaesthesiology1 site in 1 country126 target enrollmentStarted: September 22, 2020Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 126
- Locations
- 1
- Primary Endpoint
- Duration of effective post operative analgesia
Study Overview
Brief Summary
This study will compare the analgesic efficacy of two dose of Dexamethasone as adjuvant to Levobupivacaine in ultrasound guided supraclavicular brachial plexus block for upper limb surgeries
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients belonging to ASA I and II Mallampati grade 1 and 2 posted for upper limb surgeries.
Exclusion Criteria
- •Coagulopathies (INR>1.5) Infection at site of block A compromised lung function at opposite side of block like pneumothorax hemothorax pneumonectomy Hypersensitivity to Local anaesthetics or Dexamethasone Patients refusal or inability to communicate.
Outcomes
Primary Outcomes
Duration of effective post operative analgesia
Time Frame: 24 hours post operative period
Secondary Outcomes
- Time of onset of sensory and motor block
- Duration of sensory and motor block(24 hours post operative period)
- VAS score(24 hours post operative period)
- Incidence of post operative nausea vomiting(24 hours post operative period)
- Rate of infection neurologic complication hyperglycemia(24 hours post operative period)
Investigators
Study Sites (1)
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