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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: 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.

NCT ID: NCT05205616 Completed - Fracture Clinical Trials

Trial of Bilateral Sagittal Split Osteotomy Induced Paresthesia Using Ultrasonic vs. Reciprocating Saw Instrumentation

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

The aim of this prospective study is to analyze the postoperative paresthesias experienced in patients who undergo bilateral sagittal split osteotomies (BSSO) using an ultrasonic saw, versus a reciprocating saw. Patients included in the study are ages 15-45 scheduled to undergo BSSO surgery at the University of California, San Francisco. One side of the patient's mandible will be instrumented with either the Stryker Sonopet ultrasonic saw or traditional reciprocating saw, while the other side will receive the remaining intervention (determined via randomization on the day of surgery). Patient paresthesias will then be analyzed on each side for 3 months postoperatively (at postoperative days: 1, 7, 14, 28, and 84). Sensory examinations will be carried out by blinded examiners using von Frey hairs and two point discrimination testing. Patients will also subjectively rate their sensation on each side. The results will then be analyzed to determine if patient paresthesias, including the severity and duration, differed depending on which instrument was used, the ultrasonic or reciprocating saw.

NCT ID: NCT05114642 Completed - Clinical trials for Class III Malocclusion

The Effect of Orthopedic Face Mask Use on Head Posture and Pharyngeal Airway

Start date: November 30, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate the changes in head posture, position of the hyoid bone, pharyngeal airway and cervical posture after the use of Petit type face mask in patients with skeletal class III malocclusion (ANB angle < 0) with ongoing growth. No other study was found in the literature in which head posture, cervical posture, and hyoid bone position were evaluated after the use of a face mask and compared with a control group consisting of patients of the same age group and the same malocclusion.

NCT ID: NCT04911400 Enrolling by invitation - Clinical trials for Class III Malocclusion

Effects of Class III Elastics on Stability of Orthopaedic Class III Correction

Start date: July 22, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of adding elastics to orthodontic retainers on the stability of class III correction and whether it reduces the need for jaw surgery.

NCT ID: NCT04905004 Recruiting - Clinical trials for Class II Division 1 Malocclusion

Efficiency of Canine Retraction Using Different Reactivation Intervals

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

Canine retraction after 1st premolar extracion into the extraction space is a routine treatment in orthodontics. Orthodontic patients requiring first premolar extraction, canine retraction and maximum anchorage were recruited for this randomized controlled trial. A search of the literature did not indicate the ideal frequency of elastomeric chain reactivation for optimum canine retraction. The study was approved by the ethical committee. The first premolars were extracted. Elastomeric chains were used to retract the canine distally into the 1st premolar space. The optimum reactivation interval was evaluated regarding the efficiency of treatment in terms of rate of canine retraction, canine tipping and rotation, root resorption and pain at the intervals of 2, 4, 6 and 8 weeks. Three dimensional imaging, as well as digital scanning were the methods for data collection.

NCT ID: NCT04887974 Completed - Clinical trials for Class II Malocclusion

Canine Retraction With Temporary Anchorage Devices

Start date: April 2, 2016
Phase: N/A
Study type: Interventional

Various malocclusions require the extraction of the first premolars and retraction of the canines with the need for maximum anchorage. If the canines are pulled into the extraction space using the molar teeth for support, unwanted tooth movement occurs. This study aims to evaluate the effect of temporary anchorage devices and power arms, which are auxiliary orthodontic appliances in reducing undesirable tooth movements.

NCT ID: NCT04863404 Recruiting - Clinical trials for Class III Malocclusion

Evaluation of the Treatment Effects of Tooth Borne Versus Bone-anchored Protraction Procedures in Class III Patients With Maxillary Deficiency

Start date: June 15, 2020
Phase: N/A
Study type: Interventional

The aim of this prospective randomized controlled clinical study is to compare the effects of bone-anchored and tooth borne maxillary protraction on dentofacial structures in skeletal Class III patients.

NCT ID: NCT04825951 Completed - Clinical trials for Malocclusion, Angle Class III

Dentofacial Effects Of Two Non-Compliance Appliances In The Treatment Of Growing Skeletal Class III Patients

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

Early orthodontic treatment of Class III malocclusions with skeletal and dentoalveolar imbalances, represents a continuous dilemma. This difficulty starts from their meticulous diagnosis and treatment planning till reaching satisfactory results and finally stability. Some appliances could be used to correct growing skeletal Class III patients, improving the skeletal and dentoalveolar relationships, creating proper conditions for final orthodontic treatment, more importantly avoiding surgery. These appliances remove patient compliance from the equation.

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.