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Application Of Dentapen In Dental Local Infiltration Anesthesia

NCT07431801 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-02-25

No results posted yet for this study

Summary

The goal of this clinical study is to compare patients' self-reported pain and mental stress during infiltration anesthesia between conventional syringe and Dentapen.

Outcome 1: VAS score of self-reported pain during dental anesthesia Outcome 2: Heart rate variability during dental anesthesia

Conditions

  • Healthy Participants
  • Tooth Extraction
  • Orthodontic Patients

Interventions

DEVICE

computer controlled local anesthesia delivery device (Dentapen)

The participants were delivered local anesthesia using a computer-controlled local anesthesia delivery (CCLAD) device.

DEVICE

Control

Conventional syrine was used to administer local anesthesia. Participants in this group would received manual anesthesia.

Sponsors & Collaborators

  • Son Hoang Le

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-08-01
Primary Completion
2025-02-01
Completion
2025-02-01
FDA Device
Yes

Countries

  • Vietnam

Study Locations

More Related Trials

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 NCT07431801 on ClinicalTrials.gov