Efficacy of conventional syringe, insulin syringe and deception needle in reduction of anxiety and pain during administration of local anaesthesia in childre

Not Applicable

Completed

• Conditions: Health Condition 1: F419- Anxiety disorder, unspecifiedHealth Condition 2: K041- Necrosis of pulpHealth Condition 3: K040- Pulpitis

• Registration Number: CTRI/2022/01/039554
• Lead Sponsor: Department of Pediatric and Preventive Dentistry

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-01-31
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 45

Inclusion Criteria

1. Children between the age group of 6-12 years.

2. Children who require infiltration anaesthesia in the maxillary arch for restorative, pulp therapy or extraction work.

3. Children who have never experienced dental injection.

4. Patients who are willing to undergo treatment.

Exclusion Criteria

1. Children with systemic diseases and special health care needs.

2. Patients allergic to contents of local anaesthesia.

3. Patients who require emergency treatment.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in Anxiety LevelsTimepoint: Pre and Post Intervention

Secondary Outcome Measures

Name	Time	Method
Pain PerceptionTimepoint: Post Intervention