Health Condition 1: O- Medical and Surgical Health Condition 2: T07- Unspecified multiple injuries
Conditions
Interventions
Intervention1: INFRACLAVICULAR BRACHIAL PLEXUS BLOCK: Regional anaesthesia is comparatively safer and does not involve the potential side effects and complications that may arise from sedation and gen
Sponsors
vydehi institute of medical sciences and research centre
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients of either sex, aged 21-60 years, undergoing elective upper limb surgeries. 2. Patients belonging to American Society of Anesthesiologist (ASA) physical status I, II. 3. Patients within the weight range of 50-80kgs and within normal BMI.
Exclusion criteria
Exclusion criteria: 1. Patient refusal for the study. 2. Patients with coagulopathy or on anticoagulants. 3. Patients with pre-existing neuropathy involving brachial plexus. 4. Patients who have undergone prior surgeries of the infraclavicular fossa. 5. Patients with localized skin infections at site of block. 6. Patients with hypersensitivity to local anaesthetic
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To evaluate and compare the onset for sensory blockade. 2.To evaluate and compare the onset for motor blockade. 3.To evaluate and compare the duration of sensory blockade. 4.To evaluate and compare the duration of motor blockade. Timepoint: 5 mins 10 mins 15 mins 20 mins 25 mins 30 mins 1 hour 2 hours 3 hours 6 hours 12 hours 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To assess hemodynamic variables. 2. To identify adverse effects to the drugs. Timepoint: hemodynamic variables are monitored in patients who receive the block for a duration of 24 hours & the at an interval sterting with 0min, 15min, 30min, 45min, 1hr, 2hrs, 3hrs, 6hrs, 12hrs & 24hrs Adverse effects are noted upto a duration of 24hours if any | — |
Countries
India
Contacts
Public ContactDr. Pramathesh A
Department of Anaesthesiology
Outcome results
None listed