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

Not Applicable

• Conditions: K02; Dental caries

• Registration Number: DRKS00005740
• Lead Sponsor: GC Europe N.V.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-03-14
• Study Completion: 2015-12-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting stopped after recruiting started
• Sex: All
• Target Recruitment: 130

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

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.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
Failure rate of all fillings.