Ankylosed Teeth Treatment by Bone Orthodontic Treatment

NCT ID: NCT02337153

Last Updated: 2019-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-04-07

Study Completion Date

2021-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Codify the treatment of teeth by stiff Corticotomy technique. Evaluate the duration of treatment and tooth movement.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Codify the treatment of teeth by stiff Corticotomy technique. Evaluate the duration of treatment and tooth movement.

During treatment the teeth by stiff Corticotomy, millimeter measurements are performed on a cohort of patients with this pathology. These measures take place during normal clinical phases and on all media such as, plaster models, photographs and radiological examinations performed at the beginning, during and at the end of treatment.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Ankylosed Teeth

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patient in need of orthodontic treatment and presenting one or more teeth stiff
* Can meet the requirement of orthodontic treatment (attendance, quality of brushing)
* Showing no indication against General Surgery

Exclusion Criteria

* A patient against indication for orthodontic treatment : Root resorption of teeth adjacent to stiff teeth, Dental anchoring Deficiency by multiple agenesis or agenesis of the adjacent teeth to teeth stiff, Loss of periodontal support or active periodontal disease
* A patient against indication to treatment with Corticotomy : General Pathology against indicating surgery, Proximity root with no possibility of improvement orthodontic preparation
* Inability to maintain a good level of oral hygiene and good cooperation.
Minimum Eligible Age

13 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Firm Orthodontics - Mauguio - French

UNKNOWN

Sponsor Role collaborator

Universitat Internacional de Catalunya

OTHER

Sponsor Role collaborator

University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Philippe BOUSQUET, MCU PH

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Montpellier

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

UHMontpellier - AHU CSERD

Montpellier, , France

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Philippe BOUSQUET, MCU PH

Role: CONTACT

0613212053

Matthieu RENAUD

Role: CONTACT

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Philippe BOUSQUET

Role: primary

Matthieu RENAUD

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

9367

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.