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Evaluation of the Patient Experience With a Surgically-assisted Acceleration Method of Orthodontic Treatment

NCT05250921 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2022-02-22

No results posted yet for this study

Summary

The duration of orthodontic treatment is one of the exacerbation causes of orthodontic pain. Several methods have been suggested to reduce the duration of orthodontic treatment classified to surgical and non-surgical methods.

Researches used minimally invasive surgical methods like corticision, piezocesion, disicion, micro-osteoperforation, and piezopuncture indicated that most of these methods can accelerate dental movement by 20 - 40% without causing additional pain as a result of using those methods.

Applying corticision on the lower anterior teeth using a surgical blade and a hammer may accelerate tooth alignment during orthodontic treatment. This study consists of two groups, patients will be randomly assigned to one of these two groups.

Conditions

  • Crowding, Tooth

Interventions

PROCEDURE

Corticision

Corticision will be performed to enhance teeth alignment.

DEVICE

Conventional fixed appliance

No surgical intervention is going to be applied to the patients in this group.

Sponsors & Collaborators

  • Damascus University

    lead OTHER

Principal Investigators

  • Mohamad Radwan Sirri, DDS MSc · Department of orthodontics, Damascus University, Syria

  • Ahmad S Burhan, DDS MSc PhD · Professor of Orthodontics, Department of Orthodontics, University of Damascus Dental School

  • Mohammad Y Hajeer, DDS MSc PhD · Professor of Orthodontics, Department of Orthodontics, University of Damascus Dental School

  • Fehmieh R Nawaya, DDS MSc PhD · Associate Professor, Department of Pediatric Dentistry,Syrian PrivateUniversity

  • Rashad MT Murad, DDS MSc PhD · Professor of Toxins and Pharmaceutics, University of Damascus, Faculty of Pharmacology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-09
Primary Completion
2020-01-12
Completion
2020-08-26

Countries

  • Syria

Study Locations

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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 NCT05250921 on ClinicalTrials.gov