None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Participants of all gender aged between 19-60 years 2. Patients requiring intravenous cannulation 3. Only participants with American society of anesthesiologist physical status 1 and 2 are included 4. Patients undergoing elective surgery
Exclusion criteria
Exclusion criteria: 1. Patients who are unwilling or opposed 2. Coagulopathy or bleeding disorders 3. A history of allergic reactions to anesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the pain intensity experienced by adult patients during intravenous cannulation after application of EMLA CreamTimepoint: done in ward and pre-operative setting applied and kept for 30 minutes and after cannulation pain scales are assesed | — |
Secondary
| Measure | Time frame |
|---|---|
| o evaluate the pain intensity experienced by adult patients during intravenous cannulation after application of Lidocaine HCLTimepoint: done in ward and pre-operative setting applied and kept for 30 minutes and after cannulation pain scales are assessed;To compare the pain intensity experienced by adult during intravenous cannulation after application of either EMLA cream or Lidocaine HCL padded dressingTimepoint: After cannulation and after taking VAS and VDS scale will compare takes less than 5 minutes | — |
Countries
India
Contacts
Yenepoya Medical College hospital