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The Research and Development and Translation of a New Type of Pressure Film Retainer Design and Manufacturing System Based on Artificial Intelligence

The Research and Development and Translation of a New Type of Pressure Film Retainer Design and Manufacturing System Based on Artificial Intelligence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099497
Enrollment
Unknown
Registered
2025-03-25
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Dental Malocclusion

Interventions

Group A: Full-time retention using a Hawley retainer:Hawley retainer
Group B: Full-time retention using a fixed lingual retainer:fixed lingual retainer
Group C: Full-time retention using a pressure-formed retainer made with traditional methods:pressure-formed retainer made with traditional methods
Group D: Full-time retention using a pressure-formed retainer fabricated by an automated manufacturing system.:pressure-formed retainer fabricated by an automated manufacturing system

Sponsors

Shanghai Stomatological Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The brackets have not been removed after non-extraction fixed orthodontic treatment; 2. Have good oral hygiene status, no untreated caries, periodontal disease or other oral diseases that may affect the results of the experiment; 3. I or my guardian should be able to understand the experimental process and be willing to actively cooperate with the completion of intraoral scanning and related data provision; 4. No contraindications to intraoral scanning, such as allergy to scanning equipment materials, severe swallowing reactions, etc.; 5. I agree that my intraoral scan data will be used for research purposes and will be able to provide complete pre- and post-treatment data.

Exclusion criteria

Exclusion criteria: 1.Orthodontic treatment has not been completed; 2.Have active periodontal disease, untreated dental caries, or other oral diseases that may affect the experimental results; 3.There are large areas of restorations, implants, or other hardware in the oral cavity that may affect the accuracy of intraoral scanning; 4.The applicant or his/her guardian is unwilling to cooperate with the experiment, or unable to understand the experimental process; 5.Inability to provide complete pre- and post-treatment intraoral scan data, or refusal of data to be used for research; 6.Concurrent participation in other clinical studies that may affect the results of this study.

Design outcomes

Primary

MeasureTime frame
PAR Index;

Countries

China

Contacts

Public ContactZhicheng Gong

Shanghai Stomatological Hospital, Fudan University

387888827@qq.com+86 13761806588

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026