Effect of Low Level Laser Therapy on Root Resorption During Orthodontic Intrusion of Maxillary Incisors

January 28, 2023 updated by: Youssri Mahmoud Ahmed Saleh, Al-Azhar University

Effect of Low Level Laser Therapy on Root Resorption During Orthodontic Intrusion of Maxillary Incisors: A Comparative Clinical Study

The present study will be directed to evaluate the effect of low-level laser therapy on root resorption during orthodontic intrusion of upper incisors.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

18

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Naşr, Egypt
        • Al Azhar Univertsity

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 16 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients with age range between 12-16 years.

    • Overbite > 40% indicated for maxillary intrusion.
    • Mild to moderate crowding of upper incisors.
    • All permanent teeth erupted (excluding 3rd molars).
    • No previous orthodontic treatment.
    • Good oral hygiene with no previous periodontal surgery

Exclusion Criteria:

  • Transverse and/or vertical skeletal dysplasia or craniofacial malformation.

    • Retained primary or missing permanent teeth in the maxillary anterior area, and any kind of tooth/root shape anomaly.
    • Patients with root resorption, impacted canines, or dental anomalies.
    • Poor oral hygiene
    • Present or history of periodontal diseases.
    • Systemic diseases or regular use of medications that could interfere with orthodontic tooth movement.
    • History of trauma affecting the maxillary incisors.
    • Endodontically treated upper anterior teeth.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Experimental group
Will includes 9 patients who will receive intrusive arche after leveling and alignment assisted with laser with wavelength 635 nm, 6.5J/cm2,The laser will be applied to 4 points of application for each tooth two labial and two palatal started immediately after first intrusive wire then at days 3,7,14 and then every 15 day until achievement of the study objectives
The laser will be applied to 4 points of application for each tooth two labial and two palatal started immediately after first intrusive wire then at days 3,7,14 and then every 15 day until achievement of the study objectives
Active Comparator: Control group
Will includes 9 patients who will receive intrusive arches after leveling and alignment without laser application
Will includes 9 patients who will receive intrusive arches after leveling and alignment without laser application

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
linear amount of root resorption
Time Frame: change in linear root resorption at 4 months
cone beam computed linear measurements
change in linear root resorption at 4 months
volumetric amount of root resorption
Time Frame: change in volumetric root resorption at 4 months
cone beam computed volumetric measurements
change in volumetric root resorption at 4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 15, 2022

Primary Completion (Anticipated)

May 15, 2023

Study Completion (Anticipated)

December 20, 2023

Study Registration Dates

First Submitted

November 22, 2022

First Submitted That Met QC Criteria

January 28, 2023

First Posted (Actual)

February 1, 2023

Study Record Updates

Last Update Posted (Actual)

February 1, 2023

Last Update Submitted That Met QC Criteria

January 28, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 796/2193

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Root Resorption of Maxillary Incisors

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