To compare PAIN PERCEPTION in children WITH AN ELECTRONICALLY ASSISTED INJECTION SYSTEM AND CONVENTIONAL NEEDLE METHOD.
Phase 1
- Conditions
- Health Condition 1: K045- Chronic apical periodontitis
- Registration Number
- CTRI/2023/04/051267
- Lead Sponsor
- Dr Devyani Sharma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
No previous experience of dental needles.
-Patients with Frankl ++ during opd.
-Need for extraction and LA administration through infiltration.
Exclusion Criteria
-Patient with any allergy.
-History of swelling associated with the tooth
-Patient Unwilling to participate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To clinically evaluate pain perception by LA administration using electronically assisted injection system and conventional needle in children. <br/ ><br>Timepoint: 1 week
- Secondary Outcome Measures
Name Time Method To compare pain perception using electronically assisted injection system and conventional needle method during LA administration in children. <br/ ><br>Timepoint: 18months