Distractor Effect on Pain and Vitality

April 3, 2023 updated by: Alaa Mossad, Al-Azhar University

The Effect of Two and Four Activations Per Day of the Periodontal Distractor on Pain Intensity and Pulp Vitality of Maxillary Canine: Randomized Clinical Trial

The aim of the present study was to evaluate the effect of two and four activations /day of periodontal distractor on pain intensity and pulp vitality of maxillary canine.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Orthodontic therapy is generally referred to as a lengthy process because a good orthodontic treatment normally takes 18 to 24 months to finish.

Long-term orthodontic treatment has a number of disadvantages, including as poor psychosocial effects on patients, white spots, long-term enamel damage, gingival recession, and root resorption.

The rate of tooth movement that can be achieved is a major determinant of orthodontic treatment time. Many studies have been conducted to determine the pace of orthodontic tooth movement. The majority of these studies demonstrate about 1mm of tooth movement per month.

As a result, finding treatment options that reduce treatment time without compromising results is a main focus of orthodontic research.

The approaches for hastening tooth movement rely on inducing a biological tissue reaction. These procedures are classified into two types based on their level of intrusion: conservative (biological, physical, and biomechanical measures) and surgical techniques Prostaglandins are the most often used biological agents , interleukins , leukotriene , vitamin D platelet rich plasma .Mechanical or physical approach include direct electrical current , pulsed electromagnetic field , low-energy laser , and Vibration Oral surgical procedures quicken orthodontic treatment by affecting the continuity of the alveolar bone resulting in a decrease in bone density and a corresponding reduction in the bone's resistance to orthodontic tooth movement . Surgical approach depends on Regional Acceleratory Phenomenon (RAP) which is a method to speed up orthodontic treatment by accelerating bone remodeling rates and bone density. The RAP is a series of tissue reactions that occur as a damaged bone heals . These surgical methods including corticotomy , bone perforation , Distraction osteogenesis is also one of surgical methods that allow rapid canine retraction .

The technique of distraction of the periodontal ligament (PDD) was introduced for rapid tooth movement then, dento alveolar distraction (DAD) was performed to achieve rapid tooth movement using the principles of distraction osteogenesis The canine was distracted by distractor twice daily for a total about 0.4 mm per day . It has been reported in literature that up to 2 mm is distracted per day (four activations of 0.5 mm each) . The distractor was activated till the distal surface of canine became in contact with the mesial surface of second premolar.

Previous Studies of periodontal distractor have been mainly focused on the assessment of the rate and angular changes on retracted canine. No clinical study has attempted to investigate pain intensity or pulp vitality for both activation protocols of periodontal distractor during rapid canine retraction. Therefore, the aim of the present study was to evaluate the effect of two and four activations/day of periodontal distractor on pain intensity and pulp vitality of maxillary canine.

Study Type

Interventional

Enrollment (Actual)

16

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

    • Nasr City
      • Cairo, Nasr City, Egypt, 02
        • Faculty of Dental Medicine, for Girls, Al Azhar University

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Orthodontic Patients need extraction of first permanent premolar for orthodontic reasons (dentoalveolar maxillary protrusion, Class II div 1 malocclusion)
  • No history of previous orthodontic treatment
  • Absence of any systemic disease
  • Good oral hygiene and healthy gums look, with no signs of redness, edema, or bleeding during brushing (periodontal inflammation)
  • Highly motivation and cooperation

Exclusion Criteria:

  • Medically compromised patients
  • Use of medication that may affect tooth movement during the period of the study

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Canine retraction was done by periodontal distractor with two activations per day.
group 1
different activation protocols of periodontal distractor
Experimental: Canine retraction was done by periodontal distractor with four activations per day.
group 2
different activation protocols of periodontal distractor

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
pain intensity
Time Frame: 1st 48 hour after intervention (from the time of distractor placement until the end of the 2nd day)
evaluation of pain intensity by Visual Analogue scale.minimum 0 and maximum value 10.
1st 48 hour after intervention (from the time of distractor placement until the end of the 2nd day)
pain intensity
Time Frame: during each activation of the distractor,(up to 1 minute during moving the key of distractor)
evaluation of pain intensity by Visual Analogue scale.minimum 0 and maximum value 10
during each activation of the distractor,(up to 1 minute during moving the key of distractor)
pain intensity
Time Frame: up to 6 hours on the four activations group and up to 12 hours on two activations group.
evaluation of pain intensity by Visual Analogue scale. minimum 0 and maximum value 10
up to 6 hours on the four activations group and up to 12 hours on two activations group.
pulp vitality
Time Frame: before and after canine retraction (up to one month)
vitality by Electric pulp tester.positive reading is better
before and after canine retraction (up to one month)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Alaa M. Eldriny, Lecturer, Assistant Lecturer of Orthodontics,Al Azhar University, Cairo, Egypt.
  • Study Director: Ahmed A. Salama, professor, Professor of Orthodontics, Al Azhar University, Cairo, Egypt.
  • Study Director: Osama S. El-Shal, professor, Professor of periodontology Al Azhar University, Cairo, Egypt.
  • Study Director: Maha M. Mohamed, professor, Assistant professor of Orthodontics, Al Azhar University, Cairo, Egypt.

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)

February 1, 2021

Primary Completion (Actual)

August 1, 2022

Study Completion (Actual)

October 15, 2022

Study Registration Dates

First Submitted

February 27, 2023

First Submitted That Met QC Criteria

April 3, 2023

First Posted (Actual)

April 14, 2023

Study Record Updates

Last Update Posted (Actual)

April 14, 2023

Last Update Submitted That Met QC Criteria

April 3, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • PDL distractor

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.

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