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The clinical success of the permanent posterior filling alternative Equia-additional cohort.

The clinical success of the permanent posterior filling alternative Equia-additional cohort.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00005740
Enrollment
240
Registered
2014-03-14
Start date
2011-04-12
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

K02

Interventions

Group 1: Filling with a conventional Glasionomer (Fuji IX GP fast + Fuji Coat LC), 40 fillings Group 2: Filling with a modified Glasionomer + Coat (EQUIA System, Fuji IX GP Extra in combination with G

Sponsors

GC Europe N.V.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Dentate patients (no partial or full dentures, proximately three opposing zones with occlusal contacts of natural teeth in the posterior region), 2. fillings quantity is limited on the multi-surface fillings, 3. the cavity size is limited at 50% of the width of teeth, the proximal walls on the distances of the cusp tip.

Exclusion criteria

Exclusion criteria: 1. Patients with CMD dysfunction or malfunction, 2. signs of occlusal abrasion, hyperfunction, clenching will be excluded from the study. CMD-Screening, 3. Patients who withheld their paticipation will be excluded from the study, 4. none one-surface fillings, none completed or partially cusp replacements.

Design outcomes

Primary

MeasureTime frame
Differences in degree of wear and fillings fracture between both products over a five year period according to a calibrated evaluation based on FDI standard (Hickel et al 2010) beginning from Baseline.

Secondary

MeasureTime frame
Failure rate of all fillings.

Countries

Germany

Contacts

Public ContactThomas Klinke

Poliklinik f. Prothetik und Werkstoffkunde Ernst-Moritz-Arndt-Universität

klinke@uni-greifswald.de03834-867140

Outcome results

None listed

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