To evaluate the effect of Low Level lasers, external vibrating device & lignocaine gel for pain reduction during intra oralinjections
Phase 1
Completed
- Conditions
- Health Condition 1: K041- Necrosis of pulp
- Registration Number
- CTRI/2024/01/061382
- Lead Sponsor
- Dr Bollavaram Golla Aishwarya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 15
Inclusion Criteria
Children with good general health
Frankel Behaviour rating of 3 and 4
requiring administration of local anesthesia
willing to participate with parents consent are included
Exclusion Criteria
Medically compromised children,
children with active pathosis in the injection region and any history of allergy to Local Anaesthesia are excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare & evaluate the pain perception following topical application of Low Level Lasers, buzzy bee device & commercially lidocaine <br/ ><br>gelsTimepoint: 30 secs after application
- Secondary Outcome Measures
Name Time Method to evaluate any adverse effects following their applicationTimepoint: 10mins after application