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Prospective, randomized, clinical, controlled study to investigate the wear behavior of different prosthetic materials of single crowns.

Prospective, randomized, clinical, controlled study to investigate the wear behavior of different prosthetic materials of single crowns. - ZirCAD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00024377
Enrollment
69
Registered
2021-03-01
Start date
2023-01-01
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

Abrasion of artificial dental crowns in comparison

Interventions

Group 1: Crowning with all-ceramic crown lithium disilicate Group 2: Crowning all-ceramic crown zirconia Group 3: Crowning metal-ceramic crown feldspathic ceramic

Sponsors

Charité-Universitätsmedizin Berlin, Abteilung für Zahnärztliche Prothetik, Alterszahnmedizin und Funktionslehre
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - = 18 years - signed declaration of consent - pre-prosthetic treatment completed with teeth in need of crowning - antagonistic teeth present; only conservatively restored with fillings only; occlusal contacts in natural tooth structure

Exclusion criteria

Exclusion criteria: - Pregnancy at the beginning of the study - = 18 years - Pre-prosthetic treatment not completed - missing natural, antagonistic dentition and/or implant-supported, antagonistic denture - Occlusal contacts are not in natural tooth structure

Design outcomes

Primary

MeasureTime frame
Wear [µm] of metal-ceramic, silicate-ceramic and oxide-ceramic crowns.

Secondary

MeasureTime frame
1. 36-month survival rate of all-ceramic restoration. 2. occlusion control (static occlusion control + shim stock) approximal contacts 3. technical complications (surface quality, shade matching, integration of the restoration into the dentition) 4. changes in OHIP (Oral Health Impact Profile) at intervals of 6, 12, 24 and 36 months after insertion of the restoration

Countries

Germany

Contacts

Public ContactMagda Bennett

Charité-Universitätsmedizin Berlin, Abteilung für Zahnärztliche Prothetik, Alterszahnmedizin und Funktionslehre

magdalena.bennett@charite.de030 450 662 788

Outcome results

None listed

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