Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03374982 · ClinicalTrials.gov registry record · NA

Effect of the DentalVibe Injection System on Pain During Local Anesthesia Injections in Children

A NA study of Pain, sponsored by University of Nebraska.

Completed
Registry status
NA
Development phase
23
Enrollment target
1
Study location

NCT03374982: Completed NA study of Pain, sponsored by University of Nebraska.

NCT03374982 is a NA study of Pain that has completed, run by University of Nebraska. The registered enrollment target is 23 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03374982, a NA study of Pain, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
NA
Development phase
23 participants
Enrollment target
1
Study location

Study Summary

Title: Effect of the DentalVibe injection system on pain during local anesthesia injections in children. Purpose: The purpose of this study is to compare self-reported pain scale measurements using the Wong-Baker FACES pain rating scale from an experimental group (local anesthesia injection with DentalVibe system) and a control group (traditional local anesthesia injection with DentalVibe system turned off) in children. Eligibility: Children age 5-11 years old who require local anesthesia for bilateral dental treatment at University of Nebraska Medical Center (UNMC) pediatric dental clinic. Children must understand and speak English. Interventions and evaluations: Each patient will have two separate restorative appointments where the DentalVibe will be used during local anesthetic injections. One appointment the DentalVibe will be turned on and one appointment the DentalVibe will be turned off. After each injection the child will be shown the Wong Baker FACES Pain Rating Scale and asked to pick a face associated with their level of hurt during the injection. Follow-up: All children will be followed up with any necessary recommended dental treatment.

Primary Outcome

The scale includes pictures of facial expressions with correlating numerical scale of 0-10. 0 being no hurt and 10 being the worst hurt.

Conditions Studied

Interventions

  • DEVICE DentalVibe

Study Locations (1)

Nebraska

  • Children's Hospital & Medical Center Specialty Pediatric Center Dental Clinic - Omaha

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2018-02-19
Est. Completion 2019-05-20
Phase NA
University of Nebraska

407 total trials

What the finished NCT03374982 record still lists

NCT03374982 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 304-participant average among 374 other Pain trials with a reported enrollment target (92% lower).

The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 1 intervention - of which DentalVibe is the first listed.

NCT03374982 reports a single indexed study location in Nebraska.

Frequently Asked Questions

What is clinical trial NCT03374982 about?

NCT03374982 is a clinical study titled "Effect of the DentalVibe Injection System on Pain During Local Anesthesia Injections in Children". Title: Effect of the DentalVibe injection system on pain during local anesthesia injections in children. Purpose: The purpose of this study is to compare self-reported pain scale measurements using the Wong-Baker FACES pain rating scale from an experimental group (local anesthesia injection with De...

What is the current status of trial NCT03374982?

This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2018-02-19. Estimated completion is 2019-05-20.

What conditions does trial NCT03374982 study?

This clinical trial studies the following conditions: Pain.

What interventions are being tested in trial NCT03374982?

The interventions under investigation include: DentalVibe (DEVICE).

Who is sponsoring clinical trial NCT03374982?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03374982 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03374982's enrollment target sits among peer trials

23 334th of 374 higher than 41 of 374 other Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03616041 · 23 participants

    Capsule Endoscopy for Severe Hematochezia

  • NCT04348747 · 23 participants · Phase 2

    Dendritic Cell Vaccines Against Her2/Her3 and Pembrolizumab for the Treatment of Brain Metastasis From Triple Negative Breast Cancer or HER2+ Breast Cancer

  • NCT04587687 · 23 participants · Phase 2

    Brentuximab Vedotin and Bendamustine for the Treatment of Relapsed or Refractory Follicular Lymphoma

  • NCT04715022 · 23 participants · Phase 1

    Sympathetic-vascular Dysfunction in Obesity and Insulin Resistance (Vitamin C Study)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03374982, the US trial registry maintained by the National Library of Medicine. NCT03374982 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.