Adhese One F Upgrade in Direct Filling Therapy

Ivoclar Vivadent

Status: Completed

Conditions: Dental Adhesive

Treatments: Device: Adhese One F Upgrade

Study type: Interventional

Funder types: Industry

Identifiers

NCT02175368

AOFU 2012

Details and patient eligibility

About

Investigation on the clinical performance of a new dental adhesive when used in direct filling therapy after phosphoric acid etching.

Hypothesis: The new adhesive shows an acceptable clinical performance and allows a good filling quality.

Enrollment: 28 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• indication for class I or II filling
• max. 2 restorations per patient
• vital teeth
• sufficient language skills

Exclusion criteria

• dry working field cannot be established
• if the patient is known to be allergic to any of the materials' ingredients
• severe systemic diseases
• pregnancy
• non-vital or pulpitic teeth
• indication for indirect restoration

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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28 participants in 1 patient group

Adhese One F Upgrade

Experimental group

Description:

Adhese One F Upgrade (AOFU) is administered after phosphoric acid etching (etch-and-rinse protocol).

Treatment:

Device: Adhese One F Upgrade