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Clinical comparison of composite and ceramic-veneered metal-supported crowns

Clinical comparison of composite and ceramic-veneered metal-supported crowns - Adoro-Studie

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00008867
Enrollment
19
Registered
2015-07-01
Start date
2006-04-27
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

abutment teeth

Interventions

Group 1: metal-composite crown: 30 metal-composite crowns were evaluated according to the modified Ryge criteria Group 2: metal-ceramic crown: 30 metal-ceramic crowns were evaluated according to t

Sponsors

Ivoclar Vivadent AG
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: at least two adjacent single posterior crowns periodontal healthy, vital, or with root canal treatment (that was adequate), good oral hygiene

Exclusion criteria

Exclusion criteria: being under the age of 18, pregnancy, temporomandibular disorders, systemic or infectious diseases, known allergic reaction to the materials

Design outcomes

Primary

MeasureTime frame
follow-up 3.5 years: survival rate of metal-composit and metal-keramk crowns

Secondary

MeasureTime frame
follow-up 3.5 years: questionaire for esthetic appearance and chewing comfort (subjects perspective) clinical examination protocol plaque accumulation, bleeding on probing, probing depths, tooth vitality Visual examination of surface defects

Countries

Germany

Contacts

Public ContactConstanze Olms

Poliklinik für Zahnärztliche Prothetik und Werkstoffkunde

constanze.olms@medizin.uni-leipzig.de0341 9721337

Outcome results

None listed

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