Early Treatment of Anterior Open Bite Using the Rapid Molar Intruder

December 11, 2022 updated by: Damascus University

Short-term Soft and Hard Tissue Changes Following Skeletal Anterior Open Bite Treatment Using the Rapid Molar Intruder

This study evaluated the efficacy of rapid molar intruder (RMI) in treating anterior open bite in the mixed dentition. The study sample consisted of 40 patients who had a skeletal anterior open bite. The sample was allocated randomly into two groups: the RMI group and the control group. The skeletal, dentoalveolar and soft tissue changes occurring after treatment were assessed by using lateral cephalometric images.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Many appliances have been used to treat skeletal anterior open bite (AOB) malocclusion, such as removable appliances, extra-oral appliances (vertical chin cup and vertical head gear), fixed appliances, Orthognathic surgery and functional appliances. Treatment with these appliances produces soft and hard dentofacial tissue changes. Many studies have been carried out in order to study these changes.

In this study, the investigators treated AOB using RMI. Patients were divided into two groups to evaluate the efficacy of RMI.

RMI group: Rapid molar intruder was applied. Control group: Untreated control group. In order to evaluate the changes occurring, lateral cephalometric images were taken in both groups at the beginning of the treatment (T1) and after 9 months of the first cephalograms (T2).

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 years to 8 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Patients in the mixed dentition
  2. Chronological age between 8 and 12 years
  3. skeletal class I or II malocclusion
  4. Skeletal anterior open bite was assessed clinically and then confirmed radiographically: SN/GoMe was greater than 33°, MM was greater than 27
  5. No general problems
  6. Good oral health

Exclusion Criteria:

  1. Presence of periodontal diseases
  2. Presence of general diseases, syndromes or cleft lip and palate
  3. Patients with previous orthodontic treatment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Rapid Molar Intruder
Patients in this group will undergo the interventional procedure, which is the application of the rapid molar intruder appliance. This will help in correcting the open bite.
The rapid molar intruder was applied.
No Intervention: Untreated Control Group
Patients in this group will be monitored without any active treatment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the SNA angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the position of the upper jaw in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the SNB angle.
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the position of the lower jaw in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the ANB angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the spatial relationship between the upper and lower jaws in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the MM angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the amount of vertical divergence between the upper and lower jaws in the cephalometric analysis.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the SN-OCP angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the occlusion plane and the cranial base in the cephalometric analysis in the vertical direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the SN-MP angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the lower jaw plane and the cranial base in the cephalometric analysis in the vertical direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the SN-SPP angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the upper jaw plane and the cranial base in the cephalometric analysis in the vertical direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the overbite (Ovb)
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from the upper to the lower central incisors.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the overjet (Ovj)
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres Horizontally from the upper to the lower central incisors.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the Bjork sum (NS-Ar + S-Ar-Go +Ar-Go-Me)
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the UI- LI angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the upper and the lower incisor axis in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the NS-GN angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the growth pattern of the mandible in the cephalometric analysis in the vertical direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the posterior facial height (S-Go)
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from S point to GO point.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the anterior facial height (N-Me)
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from N point to Me point.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the U1-Palatal plane measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from the upper central incisor apex and the palatal plane.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the U6-Palatal plane measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from the tip of the mesial cusp of the upper first molar and the palatal plane.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the L1-GoMe measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from the lower central incisor apex and the mandibular plane.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the L6-GoMe measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres vertically from the tip of the mesial cusp of the lower first molar and the mandibular plane.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the Li-Esth measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres from the Labrale inferius and E-Line of Ricketts.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the Ls-Esth measurement
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient. This was measured in millimetres from the Labrale superius and E-Line of Ricketts.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the Nasolabial angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the nose and the upper lip in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Change in the Mentolabial angle
Time Frame: Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.
Lateral cephalometric images were taken for each patient, and this angle was measured in degrees. This angle represents the relationship between the chin and the lower lip in the cephalometric analysis in the anteroposterior direction.
Time 1: One week before the beginning of the treatment, Time 2: after nine months from the beginning of active treatment.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Mohammad Y. Hajeer, DDS,MSc,PhD, Department of orthodontics, Damascus University, Syria
  • Principal Investigator: Hammam Zeidan, DDS,MSc, Department of Orthodontics, University of Al-Baath Dental School, Hama, Syria.
  • Principal Investigator: Amjad A Hasan, DDS,MSc, Department of orthodontics, Damascus University, Syria
  • Study Director: Azzam Al-Jundi, DDS,MSc,PhD, Department of Orthodontics, University of Hama, Dental School, Hama, Syria.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 25, 2013

Primary Completion (Actual)

April 20, 2014

Study Completion (Actual)

January 20, 2015

Study Registration Dates

First Submitted

December 11, 2022

First Submitted That Met QC Criteria

December 11, 2022

First Posted (Estimate)

December 20, 2022

Study Record Updates

Last Update Posted (Estimate)

December 20, 2022

Last Update Submitted That Met QC Criteria

December 11, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • UDDS-Ortho-17-2022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Open Bite

Clinical Trials on Rapid molar intruder

Subscribe