Treatment of Retentive Teeth
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: exposure of the tooth crown.
- Who it may be relevant to
- Registry conditions: Treatment of Retentive Teeth. Basic parameters: 15 years — 25 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Russia
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Improving Orthodontic Treatment of Patients With Dental Retention
Overview
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
- Procedure exposure of the tooth crown
surgical exposure of the crown of a retentive tooth
Primary outcome measures
- treatment time [Time frame: two years]
Eligibility criteria
Inclusion criteria
- Methodology
Exclusion criteria
- patients without retentive teeth
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Russia · 1 center
- Irina — Samara
Identifiers
NCT: NCT05727670 · 8