- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02337153
Ankylosed Teeth Treatment by Bone Orthodontic Treatment (OBS)
Study of Validation of Measurements of the Movement of Stiff Treated Teeth and Orthodontic Corticotomy
Study Overview
Status
Conditions
Detailed Description
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.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Philippe BOUSQUET, MCU PH
- Phone Number: 0613212053
- Email: philipbousquet@free.fr
Study Contact Backup
- Name: Matthieu RENAUD
- Email: matt.renaud18@live.fr
Study Locations
-
-
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Montpellier, France, 34295
- Recruiting
- UHMontpellier - AHU CSERD
-
Contact:
- Matthieu RENAUD
- Email: matt.renaud18@live.fr
-
Contact:
- Philippe BOUSQUET
- Email: philipbousquet@free.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of the distal view of the tooth mesial to the stiff corner of the adjacent tooth
Time Frame: Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Millimeter caliper measurements from the point of view of tooth distal to mesial stiff angle of the adjacent tooth during care for treatment corticotomy
|
Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of the mesial angle of the ankylosed tooth to the distal (or mesial) angle of the adjacent tooth
Time Frame: Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Millimeter caliper measurements from the mesial angle of the ankylosed tooth to the distal (or mesial) angle of the adjacent tooth during care for treatment corticotomy
|
Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Change of the incisal edge of ankylosed tooth to the Incisal edge of lower incisor, In occlusion
Time Frame: Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Millimeter caliper measurements of the incisal edge of the ankylosed tooth incisal edge of lower incisor in occlusion during care for treatment
|
Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Change of free gingival margin of the ankylosed tooth to the gingival margin of the distal adjacent tooth
Time Frame: Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Millimeter caliper measurements from free gingival margin of the ankylosed tooth to the gingival margin of the distal adjacent tooth during care for treatment corticotomy
|
Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Change of free gingival margin of the ankylosed tooth to the gingival margin of the mesial adjacent tooth
Time Frame: Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Millimeter caliper measurements from free gingival margin of the ankylosed tooth to the gingival margin of the mesial adjacent tooth during care for treatment corticotomy
|
Before orthodontic preparation, At the end of the orthodontic preparation on the day of surgery, Then 7 days, 15 days, 21 days, 30 days, 45 days, 60 days from the date of Surgery, at the end of the treatment of ankylosed teeth
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Philippe BOUSQUET, MCU PH, University Hospital, Montpellier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9367
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