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Research on Full-Digital Workflow for Complete Denture Rehabilitation in Edentulous Patients

Research on Full-Digital Workflow for Complete Denture Rehabilitation in Edentulous Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117199
Enrollment
Unknown
Registered
2026-01-21
Start date
2026-01-30
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

edentulism

Interventions

Digital group:First, wear full-mouth dentures made with digital technology for 12 weeks, followed by wearing biofunctional dentures, with a one-week washout period.
BPS group:First wear biologically functional dentures for 12 weeks, then wear full-mouth dentures made with digital technology, with a one-week washout period.

Sponsors

Peking University School and Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Edentulous patients aged 18–80 years who are candidates for complete denture rehabilitation. 2.Patients who understand and accept the procedures, costs, and potential outcomes of complete denture treatment. 3.Patients with good general health, adequate neuromuscular control, and no serious systemic diseases that would compromise treatment. 4.Patients willing to participate in the study and with demonstrated good compliance.

Exclusion criteria

Exclusion criteria: 1.Patients with single-arch edentulism. 2.Patients whose systemic or oral health status precludes complete denture rehabilitation, including those with stomatognathic system functional 3.disorders, congenital or acquired maxillofacial deformities, history of maxillofacial surgery, or facial nerve disorders. 4.Patients lacking full capacity for independent decision-making and communication.

Design outcomes

Primary

MeasureTime frame
Accuracy of Maxillomandibular Relationship;Denture border adaptation; Prosthesis adjustment amount;Patient satisfaction evaluation;

Secondary

MeasureTime frame
Clinical efficiency;

Countries

China

Contacts

Public ContactLin Tang

Peking University School and Hospital of Stomatology

Tldent17@bjmu.edu.cn+86 178 6519 5353

Outcome results

None listed

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