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Research and Application of Chairside Digital Restoration System Based on 3D Printing

Research and Application of Chairside Digital Restoration System Based on 3D Printing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122846
Enrollment
Unknown
Registered
2026-04-20
Start date
2024-01-06
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Dental defect and edentulism

Interventions

Resin filling group:Repairing the affected tooth with resin filling
The 3D-printed resin inlay restoration group:Repairing the affected tooth with a 3D-printed resin inlay
The conventional complete denture restoration group:Repairing with conventional complete dentures
The 3D-printed complete denture restoration group:Restoring with 3D-printed complete dentures

Sponsors

School of Stomatology, the Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Resin Inlay Group: 1.Aged >=18 years and <= 65 years, with no restriction on gender. 2.The affected teeth have at least class ? (MO or OD) caries or old restorations. After removing the caries, the remaining dental tissues have sufficient resistance to meet the needs of filling or inlay restoration. 3.The pulp vitality of the affected teeth is normal, and the response to cold and heat tests is the same as that of the control teeth. If the pulp is involved, perfect root canal therapy is required. X - rays show that the root filling is appropriate. After observation for more than 1 week, there is no (tenderness to percussion), no loosening, the fistula has disappeared, the gums are not red, swollen or tender, and the patients have no subjective discomfort symptoms. 4.The periodontal condition of the affected teeth is good. 5.The dentition is relatively complete, the occlusal relationship is basically normal, and the contralateral homonymous teeth or opposing homonymous teeth of the affected teeth exist and are healthy natural teeth. 6.In good physical health, without systemic diseases, bad habits or a history of allergies. Complete Denture Base Group: 1.Complete dentition loss for more than 3 months. According to the classification of the absorption degree of edentulous alveolar ridges, those with absorption degree at grade 1 - 2 are selected for inclusion. 2.Symmetrical face and normal mouth opening. 3.Without severe systemic diseases or psychological diseases, with good compliance, willing to accept the requirements of clinical trials and having given informed consent.

Exclusion criteria

Exclusion criteria: Resin Inlay Group: 1.Patients with gingivitis or periodontitis that is not yet fully controlled; 2.Patients who are unable to brush their teeth properly and cannot maintain good oral hygiene; 3.Patients with excessive occlusal force or bad occlusal habits such as bruxism and clenching. Complete Denture Base Group: 1.Acute or chronic temporomandibular joint disorders; 2.History of oral or maxillofacial chemotherapy; 3.Chronic mucosal inflammation, hyperplasia, or other oral pathological conditions that would complicate the trial process; 4.Other health conditions that affect the treatment of complete denture restoration.

Design outcomes

Primary

MeasureTime frame
Clinical effect evaluation;Chewing efficiency measurement;

Secondary

MeasureTime frame
Patient Satisfaction Survey;

Countries

China

Contacts

Public ContactBai Shizhu

School of Stomatology, the Fourth Military Medical University

baishizhu@foxmail.com+86 29 8477 6511

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026