Treatment of Retentive Teeth

March 22, 2023 updated by: Samara State Medical University

Improving Orthodontic Treatment of Patients With Dental Retention

The relevance of the research topic is beyond doubt, since this work is devoted to improving the effectiveness of treatment of patients with permanent teeth that have not erupted in a timely manner. Currently, this pathology occurs in 4-18% of patients seeking specialized help in a dental clinic.

The anomaly of teething, first of all, affects the anatomical, functional and aesthetic characteristics, there is an influence on the psycho-emotional state of the patient. Despite a significant number of scientific studies by domestic and foreign authors, some features of the treatment of patients with dental retention are insufficiently covered and systematized. At the moment, there is no optimal approach to the diagnosis and treatment of dental retention, as a result of which there is a question of improving the effectiveness and quality of orthodontic treatment of patients with a diagnosis of "tooth retention".

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

Detailed Description

The purpose of the study Improving the effectiveness of treatment of patients with dental retention. Research objectives

  1. To determine the frequency of occurrence of dental retention according to the patients' requests for orthodontic care;
  2. Based on the cephalometric study to identify the features of the structure of the face and bone structures in patients with dental retention;
  3. Develop and implement an orthodontic device to obtain additional space in the dentition in patients with retention;
  4. To develop and introduce into clinical practice a method for creating surgical access to retentive teeth using digital technologies.
  5. To conduct a comparative analysis of the effectiveness of our proposed improved stages of treatment of patients with dental retention with well-known methods based on gnatic and profilometric indicators.

Materials and methods of research At the first stage of our study, it is planned to examine patients aged 15-35 years who have applied for specialized

Study Type

Interventional

Enrollment (Anticipated)

30

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

  • Russian Federation
    • Самарская Область
      • Samara, Самарская Область, Russian Federation, 446185
        • Irina

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

15 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Methodology

Exclusion Criteria:

  • patients without retentive 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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: main group
This group consists of patients with dental retention who will be treated using digital technologies and devices to create a place in the dentition
Procedure: exposure of the tooth crown
surgical exposure of the crown of a retentive tooth

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
treatment time
Time Frame: two years
acceleration of treatment terms
two years

Collaborators and Investigators

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

Sponsor

Samara State Medical University

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)

September 1, 2022

Primary Completion (Actual)

January 5, 2023

Study Completion (Anticipated)

December 31, 2024

Study Registration Dates

First Submitted

February 5, 2023

First Submitted That Met QC Criteria

February 5, 2023

First Posted (Actual)

February 14, 2023

Study Record Updates

Last Update Posted (Actual)

March 23, 2023

Last Update Submitted That Met QC Criteria

March 22, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 8

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The orthodontic design developed by us will allow to create an additional place in the dentition with the subsequent extension of the retented tooth.

The introduction into the clinical stage of the method we have developed for creating surgical access will facilitate the operation process and the number of complications.

IPD Sharing Time Frame

three years

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • CSR

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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