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Comparison of traditional and digitally produced partial dentures

Comparative evaluation of clinical stability of removable partial dentures fabricated by digital and conventional workflow

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0012225
Enrollment
20
Registered
2026-07-03
Start date
2022-07-22
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

None listed

Interventions

Medical Device, Others(A cross-over comparative study on the clinical fit of partial dentures fabricated using traditional and digital (CAD/CAM) methods) : A total of 20 patients participating in the

Sponsors

Yonsei University Health System, Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult men and women aged 20 years or older · Patients with partial edentulism, or those at risk of progressing to partial edentulism · Those who have received a detailed explanation of this clinical trial, voluntarily decided to participate, and provided written consent to comply with the precautions

Exclusion criteria

Exclusion criteria: Persons unable to read the consent form · Persons with problems with the opening and closing mechanism during treatment for temporomandibular joint disorders · Persons with congenital or acquired defects in the maxilla or mandible · Persons deemed unsuitable by the Principal Investigator or supervisor based on clinically significant medical or psychiatric findings · Other persons deemed inappropriate by the Principal Investigator due to ethical concerns or potential impact on the clinical trial results

Design outcomes

Primary

MeasureTime frame
Fit evaluation

Secondary

MeasureTime frame
Perform masticatory force evaluation and occlusal analysis

Countries

Korea, Republic of

Contacts

Public ContactJimin Kim

Yonsei University Health System, Dental Hospital

jm321@yuhs.ac+82-2-2228-3167

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jul 23, 2026