ClinicalTrials.gg
CompletedNCT07581990Updated May 13, 2026

Evaluation of Treatment Outcomes of Interceptive Orthodontic Intervention for Class Iii Malocclusion Using Inclined Plane Appliance Combined With Variable Bracket Placement

An interventional study of Inclined Plane Appliance Combined With Variable Bracket Placement in Class III Malocclusion, Facemask and Inclined Plane Appliance, sponsored by Can Tho University of Medicine and Pharmacy. Completed at 1 site in Vietnam. Open to participants aged 7 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-13.

Sponsored by Can Tho University of Medicine and Pharmacy · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Jul 2025, registered May 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Not applicable
Ages
7 Years to 12 Years
Sex
All
01

Study summary

Study Title: Evaluation of Treatment Outcomes of Interceptive Orthodontic Intervention for Class III Malocclusion Using Inclined Plane Appliance Combined With Variable Bracket Placement Objective: To evaluate the clinical and radiographic outcomes of interceptive orthodontic treatment for skeletal Class III malocclusion in children Participants: Children aged 7 to 12 years diagnosed with skeletal Class III malocclusion (ANB \< 0°, Wits \< -2mm) and cervical vertebral maturation stages CS1, CS2, or CS3, treated at the Ho Chi Minh City Hospital of Odonto-Stomatology from 2025 to 2026 Methodology: This is a descriptive study with a non-controlled clinical intervention The treatment involves the application of a fixed inclined plane appliance on the mandibular teeth combined with variable bracket placement (bonded at a 180-degree rotation) on the maxillary anterior teeth to promote the forward movement of the upper incisors and stimulate maxillary alveolar bone growth Evaluation: Treatment efficacy is assessed after 6 months by comparing skeletal, dental, and soft tissue changes using standardized lateral cephalometric radiographs and Cone Beam Computed Tomography (CBCT) Success is defined by achieving a positive overjet (≥2mm), overbite (≥2mm), and an Angle Class I molar relationship

02

Conditions studied

  • Class III Malocclusion
  • Facemask
  • Inclined Plane Appliance
03

In context

Malocclusion, Angle Class III

57 studies on the registry are indexed under Malocclusion, Angle Class III; 11 are open to participants now.

This study's enrollment of 36 is above the median of 32 across 53 interventional studies indexed under Malocclusion, Angle Class III.

Browse Malocclusion, Angle Class III studies →

Lead sponsor

Can Tho University of Medicine and Pharmacy is the lead sponsor of 35 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age: Patients between 7 and 12 years old
  • Skeletal Maturity: Cervical vertebral maturation (CVM) stages CS1, CS2, or CS3
  • Diagnosis: Diagnosed with skeletal Class III malocclusion on lateral cephalometric radiographs, characterized by an ANB angle \< 0° and a Wits appraisal \< -2mm
  • Patients and their legal guardians provide to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Dental Characteristics: Absence of anterior crossbite
  • Eruption Status: Permanent maxillary central incisors have not yet erupted
  • Molar Relationship: Molar relationship is not Class III according to Edward H. Angle's classification
  • Skeletal/Growth Issues: Excessive mandibular growth
  • Congenital Conditions: Congenitally missing maxillary first molars or presence of cleft lip and/or palate
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

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You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
36 participants (actual)

Study arms

  • Experimental
    Inclined Plane and Variable Bracket placement group

    Other: Inclined Plane Appliance Combined With Variable Bracket Placement

Interventions

  • OtherInclined Plane Appliance Combined With Variable Bracket Placement

    The treatment involves a combination of a fixed inclined plane appliance on the mandibular anterior teeth and variable bracket placement (brackets bonded with a 180-degree rotation) on the maxillary incisors . This protocol aims to promote forward maxillary growth and improve the dental relationship

06

What researchers measure

Primary outcomes

  1. Treatment success of interceptive orthodontic intervention for skeletal Class III malocclusion

    Evaluation of treatment success based on clinical and radiographic criteria. Success is defined as achieving: Positive overjet (OJ ≥ 2mm) . Positive overbite (OB ≥ 2mm) . Angle Class I molar relationship . The assessment includes measuring changes in skeletal, dental, and soft tissue parameters using standardized lateral cephalometric radiographs and Cone Beam Computed Tomography (CBCT)

    Time frame: 6 months after the start of the intervention

07

Study locations

1 site
  • Department of Orthodontics, Ho Chi Minh City Dental Hospital
    Ho Chi Minh City, Vietnam
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07581990
Lead sponsor
Can Tho University of Medicine and Pharmacy
Responsible party
Sponsor
First posted
May 12, 2026
Start date
Jul 20, 2025
Primary completion
Apr 20, 2026
Completion
Apr 20, 2026
Last update
May 13, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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