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Malocclusion clinical trials

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NCT ID: NCT03279042 Completed - Clinical trials for Class II Div 1 Malocclusion

Effectiveness of Two Corticotomy Techniques in Retracting the Upper Anterior Teeth by Using Miniscrews

Start date: September 12, 2016
Phase: N/A
Study type: Interventional

This study aims to evaluate and compare the skeletal, dental and soft tissue changes, the levels of pain and discomfort and the effect on periodontal health and teeth vitality associated to traditional corticotomy and flapless corticotomy in the retraction of upper anterior teeth. 40 patients requiring extraction of maxillary first premolars and maximum anchorage to retract the upper anterior teeth will participate in the study. They will be divided randomly into two groups : flapless corticotomy (20 patients) and traditional corticotomy (20 patients). Pre-retraction, corticotomy will be performed in the maxillary anterior segment. The skeletal, dental and soft tissue changes will be performed using lateral cephalometric radiographs which will be obtained pretreatment, pre and post en-masse retraction of the anterior teeth and we will also use the dental casts to evaluate the dental changes.

NCT ID: NCT03258411 Completed - Cross Bite Clinical Trials

Evaluation Of Different Rapid Orthodontic Expansion Devices

Start date: February 10, 2015
Phase: Phase 1
Study type: Interventional

Evaluating and comparing the short term effects of different palatal expanders on the amount of palatal expansion and buccal tipping of posterior teeth. Hypothesis: H0: There is no difference in the short term effects between the different palatal expanders. H1: There is a significant difference in the short term effects between the different palatal expanders.

NCT ID: NCT03251807 Completed - Clinical trials for Malocclusion, Angle Class II

Effect of Low-Intensity Pulsed Ultrasound on Functional Treatment of Class II Malocclusion

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

This experimental study will evaluate the effect of combined treatment with low-intensity pulsed ultrasound (LIPUS) and functional appliances (twin-block) on the correction of class II malocclusion, compared with the control group treated with functional appliances (twin-block) only. The study sample will consist of 40 patients with class II malocclusion. The sample will be allocated randomly into two groups: control group and experimental group. The functional appliance (twin-block) will be applied for all patients, while the low-intensity pulsed ultrasound (LIPUS) will be applied for the experimental group only. The skeleto-dental changes occurring after functional treatment will be assessed using cephalometric radiographs; pre and post- treatment changes for each group will be evaluated individually, and the two groups will be compared.

NCT ID: NCT03240770 Completed - Malocclusion Clinical Trials

Effect of VPro5 Therapy on Clear Aligner Therapy

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

The investigators hypothesize that brief, daily application of HFA will increase the efficiency of clear aligner treatment by altering PDL metabolism without increasing pain or discomfort. The investigators will divide subjects into 5 groups changing clear aligners at different time intervals with or without HFA application for 5 minutes/day to assess the effect on: time intervals between aligners, cytokine activity, and pain perception.

NCT ID: NCT03239912 Completed - Clinical trials for Malocclusion, Angle Class II

Treatment of Class II Malocclusion Combined With Low-level Laser

Start date: July 16, 2017
Phase: N/A
Study type: Interventional

This experimental study will evaluate the effect of combined treatment with low-level laser and functional appliances (twin-block) on the correction of Class II malocclusion, compared with the control group treated with functional appliances (twin-block) only. The study sample will consist of 40 patients with Class II malocclusion. The sample will be allocated randomly into two groups: a control group and an experimental group. Functional appliance (twin-block) will be applied for all patients. Low-level laser will be applied for the experimental group only. The skeleto-dental changes occurring after functional treatment will be assessed using cephalometric radiographs; pre- and post- treatment changes for each group will be evaluated individually.

NCT ID: NCT03239275 Completed - Clinical trials for Malocclusion, Angle Class II, Division 1

Clinical Evaluation of Bio-creative Therapy for En Masse Retraction of the Maxillary Anterior Teeth

Start date: January 17, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness and efficiency of labial versus lingual biocreative therapy in achieving en masse retraction of the maxillary anterior teeth in subjects with class II malocclusion requiring upper first premolar extraction.

NCT ID: NCT03172442 Completed - Clinical trials for Class III Malocclusion

Treatment of Skeletal Class III Malocclusion Using Orthodontic Removable Traction Appliance

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

This experimental study aims to evaluate the efficiency of the orthodontic removable traction appliance in the treatment of skeletal class III malocclusion. The study sample will consist of 44 patients with skeletal class III malocclusion. The sample will be allocated randomly into two groups: experimental group and control group. The dentoskeletal changes will be assessed by using lateral cephalometric radiographs before treatment and after obtaining 3mm positive overjet.

NCT ID: NCT03159962 Completed - Malocclusion Clinical Trials

Mandibular Response After Maxillary Orthopedic Expansion in Class II Growing Subjects

Start date: January 2015
Phase: N/A
Study type: Interventional

the effectiveness of RME (Rapid Maxillary Expander) on the sagittal dental or skeletal parameters is still controversial because very little has been written regarding the behavior of antero-posterior mandibular changes in Class II growing subjects who underwent RME as the phase 1 treatment intervention. The reported significant occlusal improvement could be attributed to other reasons, ie, skeletal growth or the use of additional appliances during transition from mixed to permanent dentition. Moreover, the majority of the studies show some limits: they are not randomized, they are not prospective, and they have no control group or they use patients from growth studies as a source for the control group. The primary objective of the present investigation was to conduct a pilot randomized controlled trial (RCT) evaluating the changes in the antero-posterior mandibular position induced by bonded or banded RMEs compared with an untreated Class II control group

NCT ID: NCT03149016 Completed - Clinical trials for Class II Division 1 Malocclusion

The Use of Corticotomy for Upper Incisors Retraction

Start date: August 20, 2016
Phase: N/A
Study type: Interventional

We aim to assess the treatment outcomes following upper incisors retraction accelerated by corticotomy procedure. So, we intend to randomize orthodontic patients with class II division I malocclusion into two groups: experimental group and control group. Both groups will start orthodontic treatment. Once a 0.019*0.025-inch stainless steel wire is fully engaged to the brackets, 1st premolars will be extracted. Canines will be retracted in the conventional manner. Then, the actual evaluation period starts when the upper incisors are retracted using two different methods.

NCT ID: NCT03141788 Completed - Malocclusion Clinical Trials

Evaluation of Clear Aligner Trays to Straighten Teeth

Start date: January 30, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the efficacy of Clear Aligners to correct tooth malocclusions with the use of attachments and/or buttons, as determined by the amount of teeth movement and overall achievement goals of the treatment plan.