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Prognathism clinical trials

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NCT ID: NCT04823325 Completed - Clinical trials for Class III Malocclusion

Determining the Presence of RAP in Orthognathic Patients and Its Effect on Root Resorption by Biomarkers

RAP
Start date: January 5, 2019
Phase:
Study type: Observational

A prospective clinical trial to what extent inflammatory biomarkers are affected by the medication after orthognathic surgery in early surgical cases and whether these biomarkers affects the amount of maxillary or mandibular incisor root resorption.

NCT ID: NCT04629859 Completed - Clinical trials for Mandibular Prognathism

Orthognathic Surgeries and Pharyngeal Airway Space

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

twenty-four patients with dentoskeletal deformity of class III will be divided equally into two groups and will be subjected to orthognathic surgeries group A; will be treated by mandibular setback surgery while group B will be treated with bimaxillary orthognathic surgery in the form of mandibular setback and maxillary advancement surgeries. the total pharyngeal airway will be measured on lateral cephalometric radiographs, integrating retro-palatal and retro-glossal area, and statistically will be compared preoperative, immediate postoperative, and at 6 months post-surgically

NCT ID: NCT04376645 Completed - Clinical trials for Orthodontic Appliance

Occlusal Bite Force Changes After Surgical Correction of the Increased Vertical Dimension

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to record the OBF changes after surgical correction of mandibular prognathism in patients with or without increased vertical skeletal dimensions at different time intervals (T0: before surgery; T1: at debond; T2: 3 months post-retention).

NCT ID: NCT04316403 Completed - Clinical trials for Class II Division 1 Malocclusion

Laser-assisted Flapless Corticotomy in Accelerating Canine Retraction

Start date: February 15, 2015
Phase: N/A
Study type: Interventional

Erbium lasers have been suggested to accomplish corticotomy without flap reflection due to their attractive advantages. The current trial aimed to evaluate the efficacy of laser-assisted flapless corticotomy in accelerating orthodontic tooth movement. The secondary aim was to evaluate the patients' responses to laser application. It was postulated that canine retraction after laser-assisted flapless corticotomy would be accomplished within a shorter period compared with the conventional canine retraction method, with no significant degree of pain and discomfort.

NCT ID: NCT03976635 Completed - Clinical trials for Orthodontic Appliance Complication

Evaluation of Pain, Discomfort and Acceptance During the Orthodontic Treatment of Class III Malocclusion

Start date: February 15, 2015
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the levels of pain, discomfort and acceptance between two treatment modalities of Class III correction of growing patients in the late mixed dentition period.

NCT ID: NCT03901209 Completed - Clinical trials for Malocclusion, Angle Class III

First-In-Man Performance and Safety Evaluation of the CARLO® Device in Midface Osteotomies

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

The study product is a Cold Ablation Robot-guided Laser Osteotome (CARLO®) robotic surgery device. It is a device that removes hard tissue such as bone by means laser ablation - it is therefore an alternative to Piezo-Electric osteotomes and/or oscillating saws or other mechanical instruments for bone cutting. In this study, the CARLO device is integrated with a computer-assisted pre-operative planning and intra-operative navigation, and will be used for Patients requiring an orthognathic procedure with a mid-face osteotomy, for whom a procedure plan is defined based on preoperative imaging.

NCT ID: NCT03712007 Completed - Clinical trials for Malocclusion, Angle Class III

Comparison of Two Miniscrew Anchored Maxillary Protraction Protocols

Start date: June 9, 2017
Phase: N/A
Study type: Interventional

This study evaluates the dentoskeletal effects produced by two maxillary protraction protocols in adolescent patients. Half of participants will be treated with a tooth-borne and tooth-bone-borne expanders as anchorage in the maxillary arch. Miniscrews will be used as anchorage in the mandibular arch for both groups.

NCT ID: NCT03354442 Completed - Clinical trials for Malocclusion, Angle Class III

Treatment of Class III Malocclusion Using Modified Fixed Mandibular Retractor Appliance

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

This experimental study aims to evaluate the efficiency of the Modified Fixed Mandibular Retractor 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 untreated control group. The soft and hard tissue changes will be assessed using lateral cephalometric radiographs before the treatment and after obtaining 3mm positive overjet.

NCT ID: NCT03353116 Completed - Clinical trials for Class III Malocclusion

Assessment of Maxillary Stability in Bimaxillary Orthognathic Patients Using the Inverted Sequence Approach

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

The investigator will assess the inverted sequence approach in the treatment of class III patient undergoing bimaxillary orthognathic surgery

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.