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Malocclusion clinical trials

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NCT ID: NCT06452368 Completed - Clinical trials for Class III Malocclusion

Palatal Versus Buccal Protraction Using Plates Assisted With Facemask in Growing Class III Patients

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

to compare Palatal and buccal protraction using plates assisted with facemask in growing class III patients

NCT ID: NCT06403033 Completed - Clinical trials for Orthodontic Appliance Complication

Mini-implant-supported Twin-Block in Treating Patients With Class II Division 1 Malocclusion

Start date: September 10, 2022
Phase: N/A
Study type: Interventional

Correcting the skeletal class II using functional appliances, whether removable or fixed, always leads to skeletal and alveolar effects. However, some of these effects are unfavorable, the most significant being the loss of support in the lower dental arch. This loss of support leads to an uncontrolled labial inclination of the lower incisors and mesial movement of the lower; these dentoalveolar effects impact the degree of skeletal correction that can be achieved. Therefore, this study aimed to evaluate the skeletal and dentoalveolar effects following the use of a mini-implant-supported Twin-Block appliance compared to the conventional Twin-Block.

NCT ID: NCT06281613 Completed - Clinical trials for Skeletal Malocclusion

Comparison of AMCOP Bioactivator and High-pull Headgear in Treating Skeletal Class II Hyperdivergent Pediatric Patients

Start date: March 3, 2024
Phase:
Study type: Observational

The aim of the present study was to retrospectively compare the clinical use of high-pull headgear versus AMCOP bioactivators for hyperdivergent pediatric patients. Cephalometric radiographs from pediatric patients treated at the Unit of Orthodontics and Pediatric Dentistry, Section of Dentistry, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy and at the private practice of Dr. Cardarelli, Isernia, Italy will be collected. Cephalometric tracing from Giannì analysis will be performed at the baseline (T0) and after 18 months of treatment (T1).

NCT ID: NCT06253286 Completed - Clinical trials for Malocclusion, Angle Class I

Predictability of Part-time Wearing of Removable Clear Aligner Therapy Versus Full Time

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

14 Patients with mild to moderate crowding and spacing will be selected according to inclusion criteria. Treatment planning will be done on Maestro® software. An impression will be taken and scanned by an extra-oral scanner. The models will be 3D printed and aligner trays will be fabricated to be delivered on biweekly basis to be worn 16 hours per day for one group and 22 hours for the other group. Superimposition of the achieved clinical model over the predicted model will be done. Linear and angular measurements will be calculated for each tooth.

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: NCT06240923 Completed - Clinical trials for Malocclusion, Angle Class II

"Three Dimensional Assessment of Maxillary Molars Following Distalization Using Two Different Approaches"

Start date: January 2, 2017
Phase: N/A
Study type: Interventional

The goal of this controlled clinical trial is to compare the effects of two distalization methods supported by inter-radicular mini-screw for maxillary molars distalization in 20 adult patients with skeletal class I or moderate skeletal class II malocclusion, dental class II molar relationship, and full permanent dentition. The participants were randomly selected according to inclusion / exclusion criteria from the outpatient clinic of the Department of Orthodontics and Dentofacial Orthopedics, Faculty of dentistry, Ain Shams University, Cairo, Egypt. Selectees age was ranging from 18 to 25 years old. An informed consent has been signed by each patient before his / her enrollment in this study, where the aim , methodology, and possible complications were been clearly described in details. This research has been thoroughly reviewed by the Research Ethics Committee of the Faculty of dentistry, Ain Shams University.

NCT ID: NCT06235138 Completed - Malocclusion Clinical Trials

Jawline Improvement Using Patient-specific Angle Implants With Virtual Planning in Orthognathic Surgery

Start date: May 15, 2017
Phase:
Study type: Observational

Background: Jawline improvement is nowadays a strong patients' demand. Among patients undergoing orthognathic surgery, it remains sometimes a challenge to manage angle definition due to the classic mandibular osteotomy trait which mostly allows sagittal mandibular movements but can't modify the ramus height. A few types of osteotomies can be used to improve jawline's shape while correcting malocclusion, but they remain technically difficult and often imply the necessity for bone grafting and/or the use of a specific saw and screwdriver. The advent of computer-assisted surgical planning and computer-aided design/ computer-aided manufacturing (CAD-CAM) techniques for patient-specific implant (PSI) fabrication has enabled new methods for managing the jawline in orthognathic surgery. The aim of this study was to assess jawline improvement with patient-specific angle implants in patients undergoing orthognathic surgery with standard osteotomies.Methods: A virtual simulation of a Le Fort I osteotomy (if needed), a sagittal split ramus osteotomy with patient-specific titanium angle implants, and a genioplasty (if needed) was conducted on a preoperative three-dimensional (3D) model of each patient's skull using ProPlan CMF software (Materialise, Leuven, Belgium). Computer-assisted osteotomy saw-and-drill guides and patient-specific implants (PSIs, titanium plates and angle implants) were produced and used during the surgery. The investigators chose to focus on jawline improvement by comparing the preoperative and the post-operative 3D-photographs using the VECTRA H2 3D imagine system (Canfield Scientific, **).

NCT ID: NCT06233188 Completed - Malocclusion Clinical Trials

Effect of Customized Lateral Nasal Wall Osteotomy on the Pterygomaxillary Separation During le Fort I Down-fracture

Start date: May 3, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to show the effect of patient specific lateral nasal wall osteotomy to the pterygomaxillary separation during Le Fort I down-fracture. Participants will be divided into two treatment groups. In study group, surgery planned according to the patients' indivudial anatomy and in the conventional group, surgery planned according to mean anatomical datas. Researchers will compare patient specific lateral nasal wall osteotomy to see if it affects the pterygomaxillary junction seperation during le fort I downfracture.

NCT ID: NCT06232928 Completed - Clinical trials for Class II Malocclusion Division 1

Early Versus Late Intermaxillary Elastics in Patients With Class II Malocclusion

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

This clinical trial aimed to compare the effect of immediate light short Class II elastics versus conventional Class II elastics on the skeletal, dental and soft tissues in patients with Class II malocclusion. Participants with class II malocclusion divided into 2 groups; early group wore immediate light short Class II elastics and conventional group wore conventional Class II elastics on rigid stainless steel arch wires.

NCT ID: NCT06209125 Completed - Clinical trials for Class II Malocclusion

Evaluation of Skeletal and Dental Effect of the New Hybrid Aesthetic Functional Appliance

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

use new hybrid aesthetic functional appliance for treatment of class II div 1 malocclusion.