None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age of the patient between 18 and 70 years. 2. ASA physical status I and II. 3. Planned for upper limb surgeries with anticipated use of tourniquet. 4. Patients who desire regional anaesthesia as primary anaesthetic. 5. Weight greater than or equal to 50kg.
Exclusion criteria
Exclusion criteria: 1. Patient refusal 2. History of allergy of local anaesthetics 3. Coagulopathy or bleeding diathesis 4. History of peripheral neuropathy 5. Local skin infection 6. Baseline systolic blood pressure greater than or equal to 150 mmHg 7. Baseline diastolic blood pressure greater than or equal to 85mmHg 8. History of chronic pain syndromes 9. History of analgesic and drug use on a regular basis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to determine which technique significantly diminishes tourniquet pain in forearm surgeriesTimepoint: 2021 | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. To compare the block performance time between the two groups 3. To compare the onset of sensory and motor blockade 4. To compare the post-operative analgesic use in the first 24 hours between the two groups 5. To compare the patient satisfaction between the two groups Timepoint: 2021 | — |
Countries
India
Contacts
Kasturba Medical College, Mangalore