MedTrace Logo

The Effect of OrthoPulse™ on the Rate of Orthodontic Tooth Movement

NCT02267811 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2019-05-21

Study results available
· View outcomes & findings →

Summary

This open label study is designed to evaluate the ability of OrthoPulse™ to safely and effectively increase the rate of orthodontic tooth movement with fixed appliances.

Conditions

  • Malocclusion

Interventions

OTHER

Orthodontic Treatment

Patients are treated for orthodontic treatment by the qualified Principal Investigator (PI). Treatment and follow-up appointments per the traditional practices of the PI and dental office.

DEVICE

OrthoPulse™

Participants carry out daily OrthoPulse™ treatments at home.

Sponsors & Collaborators

  • Biolux Research Holdings, Inc.

    lead INDUSTRY

Principal Investigators

  • Peter Brawn, DDS · Biolux Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
11 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2016-06-30
Completion
2016-06-30
FDA Device
Yes

Countries

  • United States

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 NCT02267811 on ClinicalTrials.gov