Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA grade1 and 2 Forearm surgeries Weight 40-60kgs will be included in the study informed consent
Exclusion criteria
Exclusion criteria: Morbid obesity (BMI > 40 kg/m2) patient with physical status of ASA III or greater History of lung disease, cardiac disease,hepatic or renal impairment, neuromuscular disorder History of chronic pain or psychiatric disorder Drug or alcohol abuse Hypersensitivity to local anaesthetics Patients with peripheral neuropathies and coagulation disorder Patients with history of seizures Patients with history of brachial plexus injury,clavicle fracture or chest or shoulder deformities on the operative side Pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and compare the effect of ketamine versus hyaluronidase with bupivacaine on onset and duration of sensory block(duration of anaelgesia) and motor block. To evaluate and compare the effect of ketamine versus hyaluronidase with bupivacaine on hemodynamics. Timepoint: The sensory and motor block onset will be assessed every 5 minutes upto 30 minutes. Hemodynamics will be assesed at 1st,2nd,3rd,4th,5th,6th,8th,10th,12th, and 24th postoperative hour. | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢ To evaluate and compare the effect of ketamine versus hyaluronidase with bupivacaine on postoperative pain scores and rescue analgesic. Timepoint: will be assesed at 1st,2nd,3rd,4th,5th,6th,8th,10th,12th, and 24th postoperative hour. | — |
Countries
India
Contacts
subharti medical college and hospital