Maxillary Segmental Distalization with Skeletal Anchored Appliances
This study aims to evaluate how effectively skeletal anchored digitally printed appliances can move the upper back teeth in patients with class II molar and canine relation.
maxillary segmental distalization
Malocclusion+2
+ Malocclusion, Angle Class II
+ Stomatognathic Diseases
Treatment Study
Summary
Study start date: April 12, 2024
Actual date on which the first participant was enrolled.This clinical trial aims to explore the effectiveness of two different types of dental appliances used for correcting teeth alignment in the upper jaw, specifically focusing on patients who need their upper teeth moved backwards (a process known as distalization). The study targets individuals who require orthodontic treatment to achieve proper bite alignment, which is important for both functionality and aesthetics. By comparing two different approaches—one using a device anchored to the cheek side and the other using a device anchored to the palate—the study seeks to identify which technique is more effective and comfortable for patients. This could potentially lead to improved orthodontic treatments for individuals requiring significant dental corrections. Participants in this study will be divided into two groups, each receiving a different type of dental appliance. The first group will have a device anchored with small screws placed near the cheekbones, while the second group's device will use screws placed in the roof of the mouth. Both devices are designed to be bonded to the back teeth and use elastic chains to gently move the teeth into the desired position. The force applied will be carefully measured to ensure safety, and adjustments will be made during regular follow-up appointments every three weeks. The treatment continues until a proper bite alignment is achieved, at which point the devices are removed. Throughout the study, participants' progress is monitored with dental X-rays taken before and after the treatment to assess the changes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 13 to 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location