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Treatment of Retentive Teeth

Improving Orthodontic Treatment of Patients With Dental Retention

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05727670
Enrollment
30
Registered
2023-02-14
Start date
2022-09-01
Completion date
2024-12-31
Last updated
2024-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Treatment of Retentive Teeth

Keywords

dental retention, digital dentistry, surgical navigation template, 3D printing

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.

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

Interventions

PROCEDUREexposure of the tooth crown

surgical exposure of the crown of a retentive tooth

Sponsors

Samara State Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

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

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 method

Eligibility

Sex/Gender
ALL
Age
15 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* Methodology

Exclusion criteria

* patients without retentive teeth

Design outcomes

Primary

MeasureTime frameDescription
treatment timetwo yearsacceleration of treatment terms

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026