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Malocclusion, Angle Class III clinical trials

View clinical trials related to Malocclusion, Angle Class III.

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NCT ID: NCT06250127 Recruiting - Jaw Protrusions Clinical Trials

The Effectiveness of Modified 3D Printed Customized Facemask Appliance for Treatment of Class III Malocclusion

Start date: December 1, 2022
Phase: N/A
Study type: Interventional

A randomized clinical trial to introduce a modified 3D printed customized maxillary protraction facemask and evaluate its efficacy in comparison with the conventional maxillary protraction facemask therapy in correction of Class III malocclusion of young patients

NCT ID: NCT06244563 Completed - Clinical trials for Malocclusion, Angle Class III

Evaluation of Different Anchorage-supported Appliances and Expansion Procedures for Face Mask Treatment

Start date: June 8, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to assess and compare the effect of two appliances (Hybrid-Hyrax expander/ Bonded rapid maxillary expander (RME)) supported by different anchorage units and two different expansion procedures (routine rapid maxillary expansion protocol (routine)/ alternative rapid expansion and constriction protocol (alt-RAMEC)) on maxillary protraction during face mask (FM) treatment.

NCT ID: NCT05913076 Completed - Clinical trials for Maxillary Retrognathism

Class III Malocclusion and ALT-RAMEC

Start date: January 13, 2012
Phase: N/A
Study type: Interventional

Diverse viewpoints exist regarding the correlation between the conventional rapid maxillary expansion (RME) and facemask approach and the alternative RME and facemask hybrid technique (Alt-RAMEC) in terms of the degree of maxillary protraction. The findings of the study may offer a novel approach to protocol selection based on the anomaly's degree of severity. The objective of this investigation is to assess and contrast the skeletal and dentoalveolar outcomes of three distinct Alt-RAMEC techniques.

NCT ID: NCT05822271 Recruiting - Clinical trials for Malocclusion, Angle Class III

Evaluation of Surgical Outcomes of Patients Treated With the Surgery First Approach and Aligners

Start date: January 30, 2022
Phase: N/A
Study type: Interventional

The purpose of this prospective study is to compare treatment outcomes and the quality of life of skeletal Class III patients treated with conventional fixed appliances and aligners undergoing Surgery-first approach. Data will be collected through validated questionnaires: OQLQ (Orthognathic Quality of Life Questionnaire), OHIP-14 (Oral Health Impact Proļ¬le), SF-36 (Medical Outcomes Study 36 - Item Short-Form Health Survey) and IOTN (Index of Orthodontic Treatment Need).

NCT ID: NCT05713084 Active, not recruiting - Clinical trials for Maxillofacial Abnormalities

Condylar Position Changes and TMJ Functions After BSSO Mandibular Setback, Low Medial Cut.

Start date: September 28, 2022
Phase: N/A
Study type: Interventional

This study hypotheses that using low medial cut osteotomy BSSO in mandibular setback can be an efficient and effective method to limit the bony segment interferences , decreasing muscles stripping during osteotomy ,decrease condylar torque and so securing preoperative condylar position during BSSO in comparison with using high medial cut BSSO.

NCT ID: NCT05475548 Enrolling by invitation - Clinical trials for Effect of PowerScope Appliance in Treatment of Patients With Class 3 Malocclusion

Effect of Skeletally Anchored Reversed PowerScope Appliance in Orthodontic Treatment of Patients With Class III Malocclusion

Start date: December 2022
Phase: N/A
Study type: Interventional

the PowerScope appliance is found to be efficient for the treatment of class II malocclusion. Accordingly, it appears valuable to investigate the efficiency of skeletally anchored powerScope in the treatment of class III malocclusion

NCT ID: NCT05397002 Completed - Clinical trials for Class III Malocclusion

Patient Specific Intraoral Inverted-L Osteotomy Modified With Inferior Alveolar Nerve Relocation in Corrective Mandibular Surgery

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Bilateral sagittal split osteotomy (BSSO) is considered the main osteotomy design in corrective mandibular surgery, however abnormal anatomical configuration of the posterior mandible with rolled out inferior border and thin mandibular rami with cortically adherent inferior alveolar nerve may interfere with the utilization of this osteotomy. The aim of this study is to introduce a novel modification of the intraoral inverted L ramus osteotomy (ILRO) to overcome these limitations in mandibular setback surgery. preoperative CBCT was requested for virtual planning and fabrication of cutting and drilling guides. Cutting lines were outlined to be consisted of four cuts; lateral ostectomy to uncover and lateralize the inferior alveolar nerve (IAN), posterior cut run horizontally from the anterior border of the ramus to a point just above the mandibular foramen, two anterior vertical cuts run from the anterior end of the lateral ostectomy to the inferior mandibular border. The guide was removed and the osteotomy lines were completed then the mandibular setback was oriented and fixed using pre-bent plates osteosynthesis. Inferior alveolar nerve function was regained perfectly one year post-operatively. This procedure introduces a robust alternative to the BSSO osteotomy in some cases of mandibular setback surgery.

NCT ID: NCT05350306 Completed - Clinical trials for Class III Malocclusion

The Effects of the Chin Cup on Temporomandibular Joint and Mandibular Dimensions

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

This in vivo comparative study will evaluate the changes in the mandibular dimensions and the glenoid fossa after skeletal class III subjects' therapy by chincup appliance and compare it with an untreated class III control group. Pre and post-treatment low-dose computed tomography images will be taken before and after achieving positive overjet and undergoing 16 months of active treatment/ observation. Dimensional and volumetric changes in the mandible, condyles, and glenoid fossa will be calculated and compared to those observed in the control group.

NCT ID: NCT05280678 Completed - Clinical trials for Class III Malocclusion

Success Rate of the Miniscrews in the Mandibular Buccal Shelf

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

Stability of the orthodontic miniscrews placed in the mandible is still considered to bare higher risk of failure compared to other intraoral locations. The aim of our study was to determine the influence of the miniscrew size on their long-term stability, occurrence of oral mucosa inflammation and pain lasting over 48 hours after implantation.

NCT ID: NCT05216874 Recruiting - Clinical trials for Class III Malocclusion

The Effect of Splint Usage in Laterognathic Cl III Orthognathic Surgery Patients

TMJ
Start date: January 13, 2022
Phase: N/A
Study type: Interventional

It is crucial to maintain the anatomic condylar positions during orthognathic surgery. Condylar positions are affected directly under general anesthesia because of joint and muscle relaxation. Possible unwanted changes in the joint position may cause incorrect positioning of the jawbones. This could affect the success of the surgery in terms of function and facial aesthetics causing the need for a second surgery. Our aim is to evaluate whether the use of MR Splint has a statistically significant effect on muscle relaxation-induced condyle position deviations under general anesthesia in Class III Laterognathia patients.