Comparison of clinical outcomes and patient satisfaction with digitally and conventionally manufactured total dentures

Comparison of clinical outcomes and patient satisfaction with digitally and conventionally manufactured total dentures - TO/TU

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00039355

Enrollment

Registered

2026-02-18

Start date

2016-11-14

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Two differently manufactured total prostheses were compared.

Interventions

Group 1: Participants initially receive conventionally fabricated maxillary and mandibular complete dentures. The clinical workflow includes preliminary impressions, fabrication of custom trays, funct

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Toothless upper and lower jaw; consent form signed; of legal age; sufficient alveolar ridge

Exclusion criteria

Exclusion criteria: Participants will be excluded from participating in the study if one or more of the following criteria apply: Partial dentition in the upper or lower jaw Missing or revoked declaration of consent Minors Insufficient alveolar ridge for stable mucosa-supported full dentures Known intolerances or allergies to dental materials used

Design outcomes

Primary

Measure	Time frame
Oral health-related quality of life	—

Secondary

Measure	Time frame
A secondary endpoint is the objective clinician-rated overall denture quality (e.g., fit, retention, static and dynamic occlusion, stability, esthetics, phonetics) assessed after the predefined wearing period.	—

Countries

Germany

Contacts

Public ContactFlorian Beuer

Charité-Universitätsmedizin Berlin

florian.beuer@charite.de+4930450562702

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026