Clinical Trials Logo

Clinical Trial Summary

The main objective of the investigators' study is to assess the efficacy of a course of treatment using skeletal anchorage (MINISCREW) as compared with treatment involving dental anchorage (reference) during dentofacial orthopedic treatment.


Clinical Trial Description

Multicenter prospective study on patients aged between 12 and 50 years, requiring orthodontic treatment with premolar extractions and closure of the extraction spaces by distalization of the 6 anterior teeth. In the experimental group (50 patients) distalization will be performed using skeletal anchorage (MINISCREW). In the control group (50 patients), distalization will be by dental anchorage.

The main evaluation criterion will be extraction space closure after 8 months of treatment. Angle class I cuspid and the parallelism of the dental axes will also be taken into account. Evaluations will be made by very precise radiological analysis using 3D CT-scan. Examinations will be done before and after closure of the extraction sites and will assess treatment efficacy using skeletal anchorage versus dental anchorage. Patients will also be requested to complete a satisfaction questionnaire. The study will comprise an inclusion appointment during which patient consent will be obtained and a regular monthly appointment during the 8 months of active treatment and space closure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01025141
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact
Status Completed
Phase N/A
Start date February 25, 2009
Completion date February 20, 2014

See also
  Status Clinical Trial Phase
Completed NCT05896319 - Hyaluronic Acid Treatment of the Post-extraction Tooth Socket Healing in Subjects With Diabetes Mellitus Type 2 N/A
Recruiting NCT04367766 - Management of the Fresh Extraction Socket in the Aesthetic Area N/A
Not yet recruiting NCT06147310 - Effect Alb-PRF & A-PRF in Alveolar Ridge Preservation in Diabetes Patients - A RCCT N/A
Withdrawn NCT03197311 - A Mobile Application for Post-op Analgesic Consumption N/A
Completed NCT06165692 - The Use of Platelet-rich-fibrin in Lower Third Molar Surgery. N/A
Completed NCT02697890 - Effect of Mucograft® Seal on Post-extraction Ridge Preservation Using Bone Allograft N/A
Recruiting NCT05816707 - The Assessment of Curcuma Longa Potentials for Soft and Hard Tissue Healing in Fresh Phase 1
Completed NCT02814305 - Opioid Analgesic Use and Disposal Following Outpatient Dental Surgery N/A
Completed NCT05235048 - Single Tooth Extraction in Damaged Alveoli and Implant Site Development:TootToo N/A
Completed NCT06046976 - Piezosurgical vs Conventional Exodontia Surgery in Healthy and Patients With Diabetes Mellitus Type 2 N/A
Completed NCT02200861 - Tooth Extraction With Deep Sedation in Children: A Retrospective Study N/A
Recruiting NCT06043037 - Elamrousy Modified Approach for Socket Shield Technique N/A
Recruiting NCT06212232 - A New Piezoelectric Technique in Third Molar Surgery N/A
Completed NCT02668289 - Periodontal Phenotype Study (Tooth Extraction) N/A
Active, not recruiting NCT06140277 - Using Of Chitosan in Alveolar Ridge Preservation Phase 2
Recruiting NCT05240417 - "Pontic-shield" Technique in Alveolar Ridge Preservation N/A
Enrolling by invitation NCT05765240 - The Effects of Topical Hyaluronic Acid and Laser Application on Wound Healing in Children Phase 1
Active, not recruiting NCT02519426 - Clinical Validation of a Novel Classification for Predicting Surgical Complexity in Mandibular Wisdom Teeth Surgery N/A
Completed NCT03485664 - Acutely Infected Teeth: To Extract Or Not To Extract?
Completed NCT05830747 - Effect of Pre-emptive Dose of Prednisone Versus Placebo in Impacted Third Molar Surgery Phase 4