Health Condition 1: - Health Condition 2: S00-T88- Injury, poisoning and certain other consequences of external causes Health Condition 3: S50-S59- Injuries to the elbow and forearm
Conditions
Interventions
Intervention1: Group RDD (Ropivacaine with dexmedetomidine with dexamethasone): Patients will receive single shot ultrasound guided perineural supraclavicular brachial plexus block with 20ml of 0.5% r
Sponsors
Post Graduate Institute of Medical Education and Research,
Eligibility
Inclusion criteria
Inclusion criteria: Age group: 18-65 years ASA I and ASA II patients of both gender Patients undergoing upper limb surgery under supraclavicular brachial plexus block of less than four hour duration.
Exclusion criteria
Exclusion criteria: Patient s refusal,Hypersensitivity to the drugs used in the study, Local infection at the block site, Pre-existing neurological deficits, Bleeding Tendencies, Morbid obesity, Pregnancy, Diabetes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to first rescue analgesic requirement (In first 48 hrs) Timepoint: Time to first rescue analgesic requirement in first 48 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| Onset of sensory & motor blockTimepoint: Every 5 minutes interval during first 30 minutes;Duration of motor blockTimepoint: During first 48 hrs;Postoperative Pain scores- Numerical pain rating scale (NPRS) at predefined intervalsTimepoint: During first 48 hrs;Total analgesics in first 48 hoursTimepoint: During first 48 hrs;Rebound painTimepoint: During first 48 hrs;Quality of sleep during the first & second postoperative night Sleep-NRS scoreTimepoint: During first 48 hrs;Adverse events like bradycardia, desaturation, hypotension, hypertension, arrhythmias, sedation, agitation etcTimepoint: During first 48 hrs | — |
Countries
India
Contacts
Public ContactDr Suman Arora
PostPost Graduate Institute of Medical Education
Outcome results
None listed