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Clinical Trials/NCT05913076
NCT05913076
Completed
Not Applicable

Evaluation of the Effects of Alternating Rapid Maxillary Expansion and Facemask Use in Cases of Class III Malocclusion Caused by Maxillary Retrognathia- A Prospective, Randomized Clinical Trial

Trakya University1 site in 1 country40 target enrollmentJanuary 13, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Face Mask
Sponsor
Trakya University
Enrollment
40
Locations
1
Primary Endpoint
Evaluation of Skeletal, Dental, and Soft Tissue Angular Measurements
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Diverse viewpoints exist regarding the correlation between the conventional rapid maxillary expansion (RME) and facemask approach and the alternative RME and facemask hybrid technique (Alt-RAMEC) in terms of the degree of maxillary protraction. The findings of the study may offer a novel approach to protocol selection based on the anomaly's degree of severity. The objective of this investigation is to assess and contrast the skeletal and dentoalveolar outcomes of three distinct Alt-RAMEC techniques.

Detailed Description

Alternating rapid maxillary expansion and constriction (Alt-RAMEC) procedure is one of the most frequently used methods in the treatment of Class III cases caused by maxillary retrognathia. The objective of this investigation is to conduct a comparative analysis of the skeletal and dentofacial outcomes of three distinct techniques for maxillary protraction Following the primary recording, the patients were evaluated using bonded-type rapid maxillary expansion (RME) devices and three discrete Alt-RAMEC techniques (1, 3, and 5 weeks). Lateral cephalograms were obtained from a sample of 40 patients (18 males and 22 females) with a mean age of 10.64 ± 0.98. These images were taken both before (T1) and after the 6th month of facemask treatment (T2), and were subjected to total and local superimpositions. The Wilcoxon Sign, Kruskal-Wallis and Mann-Whitney U tests were used to evaluate the data.

Registry
clinicaltrials.gov
Start Date
January 13, 2012
End Date
August 15, 2012
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hande Uzunçıbuk

Research Assistant Dr./ Principal Investigator

Trakya University

Eligibility Criteria

Inclusion Criteria

  • Maxillary retrognathia (SNA ≤ 79°)
  • Skeletal Class III malocclusion (ANB ≤ -1°)
  • Anterior cross-bite
  • Class III molar relationship
  • Horizontal growth pattern (SN/Go-Gn \< 30°)

Exclusion Criteria

  • Previous orthodontic treatment
  • Systemic disorders

Outcomes

Primary Outcomes

Evaluation of Skeletal, Dental, and Soft Tissue Angular Measurements

Time Frame: 6 months

Changes at the maxillary advancement, teeth positions and soft tissues amount were assessed in angular level. Skeletal measurements: Angular measurements: SNA (°), SNB (°), SN/S-Gn (Y-axis)(°), SN/Go-Gn (°), Ar-Go-Gn (°), SN/Go-Ar (°), and ANB (°) were measured. Dental measurements: Angular measurements: U1 to MaxP (°) for maxillary dentoalveolar measurements; L1-MandP (°) for mandibular dentoalveolar measurements; U1-L1 (°) for interdental measurements were performed. Soft tissue measurements: Changes at the upper and lower lip assessed. Angular measurements: G-Sn-Pg' (°), Nasolabial angle (°), and Labiomental angle (°) were measured.

Secondary Outcomes

  • Evaluation of Skeletal, Dental, and Soft Tissue Millimetrical Measurements(6 months)

Study Sites (1)

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