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Evaluation of Monolithic Milled Complete Removable Dentures

Evaluation of Monolithic Milled Complete Removable Dentures

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05443048
Enrollment
10
Registered
2022-07-05
Start date
2022-09-01
Completion date
2023-08-31
Last updated
2024-12-17

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

Conditions

Complete Edentulism

Brief summary

The use of complete removable dental prostheses (CRDP) is a reliable and effective treatment option for the rehabilitation of edentulous persons. In recent years, the use of computer-aided design/computer-aided manufacturing (CAD/CAM) methods has become more popular for the fabrication of CRDPs, including subtractive methods (milling) from a prefabricated resin puck. They present various advantages compared to conventional fabrication methods, namely improved mechanical properties, superior surface characteristics, shortened manufacturing time and lower cost for the patient. However, one of the shortcomings in the manufacturing of CRDPs from a single block of resin is obtaining an adequate esthetic outcome, as the transition between the gingiva-colored (pink) and tooth-colored (white) resin is not as precise as with prefabricated prosthetic teeth which are incorporated into a denture base. A novel technology has recently been launched on the market and includes a new design of distribution of pink and white resin inside a prefabricated resin puck, which would allow a superior esthetic outcome than previous techniques. The aim of this pilot study is to assess the end result of one of the available systems used for fabricating digital dentures (Ivoclar® Digital Denture®), while using the corresponding monolithic resin puck (Ivoclar® Ivotion Denture System®), and therefore determining whether this new technique is an adequate option for treating edentulous patients.

Interventions

DEVICEIvoclar Ivotion Denture System

Fabrication of maxillary and mandibular complete removable dental prosthesis with the Ivoclar Ivotion Denture System

Sponsors

Frauke Müller
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Informed Consent as documented by signature * Healed edentulous maxilla and mandible (minimum one year since last extraction)

Exclusion criteria

* Contraindications to the medical devices used, e.g. known hypersensitivity or allergy * Vulnerable subjects * Known or suspected non-compliance, drug or alcohol abuse * Inability to follow the procedures of the investigation * Participation in another investigation with a MD in the field of dentistry * Enrolment of the investigator, his/her family members, employees and other dependent persons * Reported severe bruxism or clenching habits, clinically present oro-facial pain * Width of edentulous maxilla \> 80 mm * Width of edentulous mandible \> 80 mm * Vertical height needed for maxillary prosthesis \> 38 mm * Vertical height needed for mandibular prosthesis \> 38 mm * Depression: Geriatric Depression Scale \> 9 * Xerostomia: SSFR ≤ 0.7ml/min * Dementia: Clock-Drawing Test ≤ 5

Design outcomes

Primary

MeasureTime frameDescription
EstheticsBaseline (BL, with existing dentures)The transition between the pink and white resin will be evaluated by means of a Visual Analogue Scale esthetic score Maximum (best outcome): 1000 Minimum (worst outcome): 0

Secondary

MeasureTime frameDescription
Denture satisfactionBaseline (BL, with existing dentures)Denture Satisfaction Index: validated questionnaire with 24 questions related to 9 dimensions, by means of a Visual Analogue Scale Maximum (best outcome): 900 Minimum (worst outcome): 0
Masticatory analysisBaseline (BL, with existing dentures)Chewing efficiency will be evaluated with a two-color mixing ability test
Oral health-related quality of lifeBaseline (BL, with existing dentures)OHIP-EDENT: validated questionnaire with 19 questions related to 7 dimensions, by means of a 6-item Likert scale Maximum (worst outcome): 7 Minimum (best outcome: 0
Number of prosthetic maintenance needed3 months (T1)events such as adjustment and repair requirements will be recorded
Willingness to Pay3 months (T1)open-ended contingency valuation (CV) method of questioning with the use of a payment card. The score is the amount in Swiss Francs the participant would be willing to pay for the treatment. Maximum: no maximum Minimum: 0.
Prosthetic EvaluationDay 0 (T0, new dentures)Denture quality objectively based on the seven criteria adopted from Alfadda et al., 2014, using a scoring sheet with 16 questions, by means of a 3-item Likert scale Maximum (worst score): 48 Minimum (best score): 16

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026