The clinical success of the permanent posterior filling alternative Equia ®

Not Applicable

• Conditions: K02; Dental caries

• Registration Number: DRKS00004220
• Lead Sponsor: GC Europe N.V.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-09-06
• Study Completion: 2015-07-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 510

Inclusion Criteria

Dentate patients, no partial or full dentures, proximately three opposing zones with
occlusal contacts of natural teeth in the posterior region

Exclusion Criteria

Patients with CMD dysfunction or malfunction (signs of occlusal abrasion,
hyperfunction, clenching) will be excluded from the study. CMD-Screening form according to DGZMK record.
Participants, who may not be willing to sign the consent form, will be withdrawn to
take part in the clinical investigation (according to Declaration of Helsinki and ICH E6
(R1) GCP Guidelines, July 2002).

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Survival rate of the compared two arms in a 5 year follow up 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