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CLINICAL PERFORMANCE OF LITHIUM DISILICATE AND HYBRID CERAMIC FOR THE RESTORATION OF WORN POSTERIOR DENTITIONS – A RANDOMIZED CONTROLLED SPLIT-MOUTH TRIAL ("HC vs LD")

CLINICAL PERFORMANCE OF LITHIUM DISILICATE AND HYBRID CERAMIC FOR THE RESTORATION OF WORN POSTERIOR DENTITIONS – A RANDOMIZED CONTROLLED SPLIT-MOUTH TRIAL ("HC vs LD") - HC vs LD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00027277
Enrollment
22
Registered
2022-05-10
Start date
2022-07-12
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

Loss of Tooth Substance

Interventions

Group 1: hybrid ceramic ("HC", test) Group 2: lithium disilicate ceramic ("LD", control)

Sponsors

Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - = 18 years of age - Eroded posterior dentition - In need of increasing the vertical dimension = 1 mm (in the premolar region) - In need of minimal 4 posterior restorations (2 per side) in the maxilla and/or mandible - A signed informed consent

Exclusion criteria

Exclusion criteria: - Women who are pregnant, or breast feeding at the date of inclusion - Known or suspected non-compliance, drug or alcohol abuse - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant - Diagnosis of active bulimia nervosa or anorexia - Untreated periodontal disease - Teeth in need of a conventional full-crown restoration - Clinical signs of active bruxism

Design outcomes

Primary

MeasureTime frame
As a primary outcome, the success rate of the posterior restorations, based on the ratings of the USPHS criteria, will be compared among the two restorative materials after 5 years of function.

Secondary

MeasureTime frame
Secondary endpoints will be assessed at different time-points: Baseline, 1-year, 3-year and 5-years. - Patient related outcome measures (PROMs) evaluated with the OHIP-14 questionnaire - Periodontal and clinical parameters - Volumetric analysis of the casts - Success rates, based on the USPHS criteria - Time and costs for aftercare interventions

Countries

Switzerland

Contacts

Public ContactAlexis Ioannidis

Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin

alexis.ioannidis@zzm.uzh.ch0041 44 634 04 04

Outcome results

None listed

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