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Malocclusion, Angle Class II clinical trials

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NCT ID: NCT06430710 Completed - Deep Overbite Clinical Trials

Tooth Borne Versus Temporary Anchorage Devices (TAD) Based Intrusion Systems for the Correction of Anterior Deep Overbite

Start date: September 25, 2022
Phase: N/A
Study type: Interventional

Compare the tooth borne versus fixed orthodontic intrusive system (TADs) for the correction of anterior deep overbite

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: 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: 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.

NCT ID: NCT06209086 Completed - Clinical trials for Class II Malocclusion

Effects of Skeletal Anchored Versus Incisal Capped Twin Block Appliance in Class II Malocclusion

Start date: May 12, 2021
Phase: N/A
Study type: Interventional

: the purpose of this study was to evaluate the dento-skeletal effects of the mini-implant supported Twin Block versus the incisal capped appliance in the treatment of skeletal class II patients with mandibular retrognathism. Methods: Twenty patients with skeletal class II mandibular retrusion were included in the study. They were recruited with a random and equal allocation into 2 groups. The first group was treated with incisal capped TB without skeletal anchorage. The second group were treated with mini-implant supported TB. The mini-implants were inserted in the inter-radicular region between the mandibular second premolar and first molar. Intra-oral elastics were attached from the mini-implant to the wire hook in the canine region of the lower part of the TB and they were changed every 24 hrs. 100 to 150 gm of force was applied. Cephalometric radiographs were acquired at the beginning (T1) and end of treatment (T2). The paired-samples and independent-samples t-tests were used to evaluate and compare the changes within groups and between groups, respectively.

NCT ID: NCT06098885 Completed - Clinical trials for Third Molar Impaction

The Effect of Different Treatment Modalities of Class II Malocclusion on Upper Third Molars.

Start date: September 4, 2021
Phase:
Study type: Observational

What is the effect of the different treatment modalities (distalization versus upper premolar extraction) of class II malocclusion on the position, inclination and incidence of impaction of the upper third molars?

NCT ID: NCT06024382 Completed - Clinical trials for Class II Malocclusion

The Effect of Low-level Laser Therapy on Functional Treatment of Skeletal Class II Patients

Start date: October 26, 2022
Phase: N/A
Study type: Interventional

this is a controlled clinical trial with 2 groups of patients of class II skeletal discrepancy due to mandibular retrusion one group is treated with twin block functional appliance and the other with twin block combined with low level laser therapy ,the study aims to detect the effect of low level laser on the skeletal outcomes , dentoalveolar outcomes, rate of correction and pain during treatment

NCT ID: NCT05920525 Completed - Clinical trials for Class II Malocclusion, Division 1

Pain, Discomfort, and Acceptance During Using Electrical Stimulation to Accelerate Orthodontic Teeth Movement

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

Forty patients with class II division 1 malocclusion who will require extraction of the upper first premolars as a part of the orthodontic treatment plan will be invited to participate in the study. They will be divided randomly into two groups: the electrical group and the control group. The en-masse retraction technique will be used to retract the upper anterior teeth using mini-implants as an anchor unit to provide the maximum anchorage and Nickle-Titanium closed coil springs that will be stretched from the mini-implants to the crimpable hooks on the base wire and applied 250 g of force per side. A special removable electrical device will be used to provide electrical stimulation during the retraction phase. The levels of pain and discomfort will be self-reported using a questionnaire with visual analog scales.

NCT ID: NCT05734092 Completed - Deep Overbite Clinical Trials

Evaluation of Root Resorption During the Correction of Deep Bite With the Help of Laser Irradiation

Start date: November 15, 2019
Phase: N/A
Study type: Interventional

This study aims to investigate the effectiveness of low-level laser in reducing the resorption of the roots of the upper incisors. Participants will be recruited from patients who will attend the Department of Orthodontics and Dentofacial Orthopaedics at Damascus University. The study sample will consist of 30 patients with a deep bite who will be randomly distributed equally into two groups, 15 patients in each group, average age: 22.37±3.38 years. Mini-implants will apply between the roots of the maxillary central and lateral incisor at both sides with a loading force of 40 g on each end by using a nickel-titanium spring extending from the head of the mini-implants to a wire welded to it with two hooks. A low-level laser (Ga-Al-As) will be used with 808 nm wavelength in continuous mode, 250 milli-Watt power output, 4 Joules/point energy density, 16 s per point in the experimental group. It will be applied on the day of intrusion, then on days 3,7, and 14 of the first month, and then every 15 days starting from the second month until the end of the intrusion. In addition to adjusting the force gauge every 4 weeks until the end of the intrusion stage and reaching normal coverage will be activated every 4 weeks in both groups until normal overbite was reached.