Clinical performance of a new temporary crown and bridge material

Not Applicable

• Conditions: K00.2; K02.8; K02.9; K03.0; K03.1; K03.2; K03.6; K03.7; K03.8; K07.4

• Registration Number: DRKS00000177
• Lead Sponsor: 3M ESPE AG

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-08-28
• Study Completion: 2010-03-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

The study will include patients who
are receiving a fixed partial denture or telescopic crowns, are at least 18 years old, have given informed consent

Exclusion Criteria

Patients who
have a known allergy to constituents of the materials used, are addicted to medication, alcohol and/ or drugs, are suffering from infectious diseases (hepatitis, HIV, tuberculosis), are suffering from malignant tumors, are undergoing or have undergone radiotherapy, are pregnant or breast feeding, are not giving informed consent, are applying for renewal of a telescopic denture, that is already present

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of the number of failures of the temporary restoration being made of Protemp 4 with the number of failures of temporary restorations being made of Luxatemp® Automix Plus (Reference data)

Secondary Outcome Measures

Name	Time	Method
Colour stability, soft tissue reaction, clinical handling, accuracy of fit, outer shape, plaque accumulation, adhesion to the tooth stump and patients' opinion of the temporary restorations being made of Protemp 4 in comparison to the data of the temporary restorations being made of Luxatemp® Automix Plus (Reference data)