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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02175329
Other study ID # CAD-On
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2010
Est. completion date December 31, 2017

Study information

Verified date March 2017
Source Ivoclar Vivadent AG
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

60 bridge frameworks are CAD/CAM manufactured from zirconia-ceramic; 30 bridges are veneered with CAD/CAM fabricated lithium disilicate ceramic, 30 bridges are manually layered. The goal is to compare clinical survival , biological or technical behaviour of the restorations.


Description:

Randomized prospective controlled clinical study with three-unit posterior bridges made of zirconia-ceramic to compare veneering with manually layering or CAD/CAM fabricated lithium disilicate ceramic veneers. The hypothesis is that there is no difference in clinical survival of the restorations and no difference in biological or technical behaviour.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- single missing posterior tooth with two adjacent posterior teeth

- no acute conservative or paradontal treatment need except for the teeth to be treated in the study

- sufficient oral hygiene

Exclusion Criteria:

- known allergies to components

- bruxism

- missing antagonist tooth

- pregnancy or lactation

- missing written consent

- patients which are not expected to be compliant

- severe systemic diseases

- untreated carious lesions

- untreated parodontitis

Study Design


Related Conditions & MeSH terms


Intervention

Device:
CAD/CAM Veneering
CAD/CAM fabricated zirconia bridge framework is veneered with CAD/CAM fabricated lithium disilicate ceramic veneer
Manually layered veneering


Locations

Country Name City State
Switzerland Universität Zürich, Zentrum für Zahn-, Mund- und Kieferheilkunde Zürich

Sponsors (1)

Lead Sponsor Collaborator
Ivoclar Vivadent AG

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with clinical success Clinical success is defined as more than 95% survival of the restoration after 2 years. 2 years
Secondary Restoration quality Characterisation of the restorations according to United States Public Health Services (USPHS) criteria 1 week, 1 year, 2 years, 3 years, 4 years, 5 years