To compare the reduction of pain during iv cannulation using Lidocine spray or Buzzy device with conventional means of IV cannulatio
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/03/017967
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 105
Inclusion Criteria
1.Paediatric patients of age 8-15 years requiring I.V cannulation.
2.Informed consent
3.Patient assent
Exclusion Criteria
1.Parent refusal
2.Known allergy to any of the medication used in the study.
3.Hemodynamically unstable patients.
4.Patients who received analgesics before 4 hours of the procedure.
5.Cracked or scaly skin
6.Local bruising and redness of the skin.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the pain scores during I.V. cannulation using Conventional method, Lidocaine 10% spray and Buzzy®.Timepoint: 1-5minutes
- Secondary Outcome Measures
Name Time Method Anxiety associated with cannulationTimepoint: 1-5 minutes;Any side effectsTimepoint: 10-15 minutes;Ease of IV cannulationTimepoint: 1-5 minutes