Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere
Conditions
Interventions
Intervention1: IV lignocaine: A pneumatic tourniquet at 70 mmHg will be applied on the same arm as the intravenous cannula and the study drug will be given intravenously over 10 seconds, i.e., IV Lign
Sponsors
Sapthagiri Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: with informed consent patients of physical status ASA 1 and 2 posted for elective surgery under general anesthesia
Exclusion criteria
Exclusion criteria: patients with hypersensitivity or allergies to propofol patients with any neurological disease or focal neurological deficit pregnant woman patients on chronic antipsychotic and chronic pain medications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study is undertaken to determine the efficacy of transcutaneous electrical nerve stimulation versus lignocaine in alleviating pain on propofol injection. Severity of pain based on Verbal Rating Scale by McCrirrick and Hunter pain scaleTimepoint: Severity of pain is assessed based on Verbal Rating Scale by McCrirrick and hunter pain scale at 5seconds, 10seconds and 15seconds after propofol injection. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactDr Nikila D G
Sapthagiri Institute of Medical Sciences and Research Center
Outcome results
None listed