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Effect of Starpen Injection Device Versus Conventional Syringe During Anesthesia and Extraction of Primary Molars

NCT07156032 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2025-09-04

No results posted yet for this study

Summary

To evaluate the effect of Starpen device on pain perception during anesthesia and extraction of maxillary primary molars.

Conditions

  • Pain Perception of the New Device

Interventions

DEVICE

Starpen automatic injection device

Starpen device will be used on high speed 45-150s with the conventional carpule of articaine HCL 4% with 1:100,000 epinephrine and short needle

PROCEDURE

conventional syringe

injection will be done using conventional metal syringe with articaine HCL 4% with 1:100,000 epinephrine and short needle

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-31
Primary Completion
2026-07-31
Completion
2026-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07156032 on ClinicalTrials.gov