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Status unknownNCT02337153OBSUpdated Aug 2, 2019

Ankylosed Teeth Treatment by Bone Orthodontic Treatment

An observational study in Ankylosed Teeth, sponsored by University Hospital, Montpellier. Status unknown at 1 site in France. Open to participants aged 13 Years to 25 Years. Per ClinicalTrials.gov, last updated 2019-08-02.

Sponsored by University Hospital, Montpellier · Observational

The sponsor has not verified this record recently (last verified Aug 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
13 Years to 25 Years
Sex
All
01

Study summary

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

Read the 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.

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Conditions studied

  • Ankylosed Teeth

Keywords

  • Orthodontique Bone Stretching
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In context

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patient in need of orthodontic treatment and presenting one or more teeth stiff

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

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.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Change of the distal view of the tooth mesial to the stiff corner of the adjacent tooth

    Millimeter caliper measurements from the point of view of tooth distal to mesial stiff angle of the adjacent tooth during care for treatment corticotomy

    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

Secondary outcomes

  1. Change of the mesial angle of the ankylosed tooth to the distal (or mesial) angle of the adjacent tooth

    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

    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

  2. Change of the incisal edge of ankylosed tooth to the Incisal edge of lower incisor, In occlusion

    Millimeter caliper measurements of the incisal edge of the ankylosed tooth incisal edge of lower incisor in occlusion during care for treatment

    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

  3. Change of free gingival margin of the ankylosed tooth to the gingival margin of the distal adjacent tooth

    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

    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

  4. Change of free gingival margin of the ankylosed tooth to the gingival margin of the mesial adjacent tooth

    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

    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

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Study locations

1 of 1 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 2, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02337153
Lead sponsor
University Hospital, Montpellier
Collaborators
Firm Orthodontics - Mauguio - French, Universitat Internacional de Catalunya
Responsible party
Sponsor
First posted
Jan 13, 2015
Start date
Apr 7, 2014
Primary completion
Dec 1, 2021 (estimated)
Completion
Dec 31, 2021 (estimated)
Last update
Aug 2, 2019

Study contacts

Philippe BOUSQUET, MCU PH
Contact
philipbousquet@free.fr
0613212053
Matthieu RENAUD
Contact
matt.renaud18@live.fr
Philippe BOUSQUET, MCU PH
principal investigator · University Hospital, Montpellier

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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