Assessment of digitally manufactured maxillary full dentures using the Baltic Denture System - a clinical pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00025931

Enrollment

Registered

2021-08-12

Start date

2021-09-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

K08

Interventions

Group 1: Treatment 1 (From 1st of Sep. 21): Evaluation of the conventionally manufactured prosthesis using the practitioner questionnaire 1-3, the objective test parameters and the patient questionnai

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: To participate in this study, patients must already be fitted with a maxillary full denture, that must not be older than 4 years. In the lower jaw, full or residual teeth with a removable and / or fixed restoration are necessary up to at least the first large molar. It is also important that the patents do not have any serious problems with their current prosthesis

Exclusion criteria

Exclusion criteria: Patients are not allowed to take part in this clinical study if they have an intolerance or allergy to plastic (e.g. PMMA). In addition, the patients are not allowed to participate in the study if they do not meet the prosthetic inclusion criteria

Design outcomes

Primary

Measure	Time frame
The aim of the study is to assess the digitally manufactured maxillary full dentures of the Baltic Denture System by Merz Dental	—

Secondary

Measure	Time frame
In addition, the comparison with conventionally manufactured maxillary full dentures	—

Countries

Germany

Contacts

Public ContactAndree Piwowarczyk

Universität Witten/Herdecke

andree.piwowarczyk@uni-wh.de02302 926665

Outcome results

None listed

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