Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Weight 50-80 kilograms ASA grade I and II All patients scheduled for elective upper limb surgeries under supraclavicular brachial plexus block
Exclusion criteria
Exclusion criteria: Patient refusal for consent Age less than 18 years and more than 60 years ASA grade III and IV Patients with abnormal coagulation profile Patients with local skin site infections Patient allergic to study drugs Pregnant and lactating mothers Failure or inadaequate supraclavivular block patient will be excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effects of Dexmedetomidine and Dexamethasone as a perineural adjuvant to 0.5% Bupivacaine in supraclavicular brachial plexus block.Timepoint: UPTO 6 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the onset time and duration of sensory and motor blockade of Dexmedetomidine with 0.5% Bupivacaine for Supraclavicular brachial plexus block. To assess the onset time and duration of sensory and motor blockade of Dexamethasone with 0.5% Bupivacaine for Supraclavicular brachial plexus block. To observe time required for Rescue Analgesia in both the groups. To compare the observations of the 2 groups. Timepoint: upto 6 hours | — |
Countries
India
Contacts
Peoples College Of Medical Sciences and Research Centre Bhopal