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A prospective randomized clinical study comparing the resistance control efficacy of four-dimensional and three-dimensional orthodontic systems

A prospective randomized clinical study comparing the resistance control efficacy of four-dimensional and three-dimensional orthodontic systems

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123731
Enrollment
Unknown
Registered
2026-04-29
Start date
2026-03-28
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abnormalities in the morphology, function or position of teeth, jawbones and facial structures during development, manifested as misaligned teeth, disordered occlusal relationships and asymmetrical facial appearance, etc.

Interventions

Damon group:Damon orthodontic appliance
MBT group:MBT orthodontic appliance
PASS group:PASS orthodontic appliance

Sponsors

Stomatological Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.Voluntarily cooperate with this research and sign the informed consent form for the research (for minor subjects, it must be signed by their legal guardians); 2.The diagnosis is clear. Comprehensive fixed orthodontic treatment is required, and the treatment plan involves extracting two first premolars from both the upper and lower jaws. 3.Gender is not limited. Age range: 12 to 35 years old. 4.The molar relationship is Angle Class I or Angle Class II;

Exclusion criteria

Exclusion criteria: 1.Cases where grinding teeth is required for distal movement to create a gap; 2.There is a history of tooth extraction in the molar area (excluding the third molar). 3.There is a molar "scissors bite" relationship; 4.Has received orthodontic treatment or orthognathic surgery treatment; 5.There are missing or impacted teeth (except for the third molars). 6.Suffering from systemic severe diseases (requiring long-term medication), severe periodontitis, congenital cranio-maxillofacial deformities or syndromes; 7.Long-term history of smoking or heavy drinking; 8.Pregnancy or lactation; 9.Receive other clinical trial intervention measures or other trial drugs during orthodontic treatment.

Design outcomes

Primary

MeasureTime frame
Mesial displacement of maxillary first molar (mm);

Secondary

MeasureTime frame
The variation in the near-distal axial inclination of the maxillary canines and the first molars (°);The improvement effect of occlusion;The vertical variation (mm) of the maxillary central incisors and the maxillary first molars;Retraction of the maxillary central incisors (mm);The variation in the width between the bilateral maxillary canines and the width between the first molars (mm);Torque variation (°) of the maxillary central incisors, canines and first molars;

Countries

China

Contacts

Public ContactLiu Chufeng

Stomatological Hospital of Southern Medical University

307488118@qq.com+86 20 34400329

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026