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NCT05334433 Clinical Trial

Child Behavior After Local Anesthetic Injection Using Needless Systems

Child Behavior Clinical Trial

Official title:
Assessment of Child Behavior and Soft Tissue Reaction After Local Anesthetic Injection Using Needle Versus Needless Systems

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05334433
Other study ID # 3399444
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 20, 2022
Est. completion date May 20, 2023

Study information
Verified date September 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effect of needless injection (comfort in ject) on child behavior and its effect on adjacent oral mucosa and soft tissue in children during local anesthesia injection in comparison to the conventional injection technique

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date May 20, 2023
Est. primary completion date December 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 8 Years
Eligibility Inclusion Criteria: - According to Wright's classification of child behavior, children are classified as cooperative or possibly cooperative. - Children who are medically fit. - Children who are capable of interacting on a mental level. - Children between the ages of 6 to 8. - First dental visit. Exclusion Criteria: - Children who struggle with behavioral control (uncooperative). - Children who have a history of allergic reaction to local anesthetic drugs. - Parental rejection for participation.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Local anesthesia injection
Local anesthesia administration

Locations
Country Name City State
Egypt Faculty of Dentistry, Cairo University, Cairo, Egypt Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Child behavior (Feeling pain during injection) (Binary Yes/No) Pain perception during LA injection During injection (Immediate) (No follow up)
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