Treatment of Retentive Teeth

Sponsor

Samara State Medical University (Other)

Overall Status

Enrolling by invitation

CT.gov ID

NCT05727670

Collaborator

(none)

Enrollment

Location

Arm

Anticipated Duration (Months)

1.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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".

Condition or Disease	Intervention/Treatment	Phase
Treatment of Retentive Teeth	Procedure: exposure of the tooth crown	N/A

Detailed Description

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

To determine the frequency of occurrence of dental retention according to the patients' requests for orthodontic care;
Based on the cephalometric study to identify the features of the structure of the face and bone structures in patients with dental retention;
Develop and implement an orthodontic device to obtain additional space in the dentition in patients with retention;
To develop and introduce into clinical practice a method for creating surgical access to retentive teeth using digital technologies.
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 Design

Study Type:

Interventional

Anticipated Enrollment :

30 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Intervention Model Description:

At the first stage of our study, it is planned to examine patients aged 15-35 years. The examination will be carried out according to the scheme including the main (clarification of complaints, anamnesis collection, external examination, examination of the oral cavity and teeth) and additional examination methods (anthropometric examination of diagnostic models of dentition, cone-beam computed tomography of the head, orthopantomography, telerentgenography of the head, electrodontodiagnostics, determination of the area of occlusal contacts). At the second stage of our study, it is planned to sample the results with the division of patients into the main and control groups. The main group will include patients who will receive orthodontic treatment according to the method we have proposed. The control group will include patients whose treatment will be carried out according to the standard methodAt the first stage of our study, it is planned to examine patients aged 15-35 years. The examination will be carried out according to the scheme including the main (clarification of complaints, anamnesis collection, external examination, examination of the oral cavity and teeth) and additional examination methods (anthropometric examination of diagnostic models of dentition, cone-beam computed tomography of the head, orthopantomography, telerentgenography of the head, electrodontodiagnostics, determination of the area of occlusal contacts). At the second stage of our study, it is planned to sample the results with the division of patients into the main and control groups. The main group will include patients who will receive orthodontic treatment according to the method we have proposed. The control group will include patients whose treatment will be carried out according to the standard method

Masking:

None (Open Label)

Masking Description:

development of a method for the treatment of extension of s with acceleration of treatment time

Primary Purpose:

Treatment

Official Title:

Improving Orthodontic Treatment of Patients With Dental Retention

Actual Study Start Date :

Sep 1, 2022

Actual Primary Completion Date :

Jan 5, 2023

Anticipated Study Completion Date :

Dec 31, 2024

Arms and Interventions

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

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

Outcome Measures

Primary Outcome Measures

treatment time [two years]
acceleration of treatment terms

Eligibility Criteria

Criteria

Ages Eligible for Study:

15 Years to 25 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Methodology

Exclusion Criteria:

patients without retentive teeth

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Irina	Samara	Самарская Область	Russian Federation	446185

Sponsors and Collaborators

Samara State Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Samara State Medical University

ClinicalTrials.gov Identifier:

NCT05727670

Other Study ID Numbers:

First Posted:

Feb 14, 2023

Last Update Posted:

Feb 14, 2023

Last Verified:

Feb 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Yes

Plan to Share IPD:

Yes

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Samara State Medical University

dental retention

digital dentistry

surgical navigation template

3D printing

Study Results

No Results Posted as of Feb 14, 2023