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Clinical Evaluation of Adhese Universal DC in the Indirect Restorative Therapy

Not Applicable
Terminated
Conditions
Dental Caries
Defective Tooth Restorations
Interventions
Device: Adhese Universal DC
Device: Adhese Universal
Registration Number
NCT04475679
Lead Sponsor
Ivoclar Vivadent AG
Brief Summary

A post market clinical follow up study (PMCF) with Adhese Universal DC is planned to ensure the safety and efficacy of the product. It is a study with two arms. Inlays and onlays for molars and premolars will be luted with Adhese Universal DC or Adhese Universal.

Detailed Description

This study aims to assess the long-term safety of Adhese Universal DC in terms of tooth vitality and failure rate of placed restorations. Tooth vitality is an indicator for the health status of the dental pulp. A vitality test is performed to acquire information about the vitality of teeth. A healthy dental pulp offers a positive response to the vitality test. Once the dental pulp is injured an irreversible inflammatory reaction starts with a possible necrosis of the dental pulp. Pulpa necrosis is followed by a negative response to the vitality test.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Age: 18-65 years
  • Indication for indirect restorations (inlay, onlay) in molar or premolar - replacement of insufficient fillings (e.g. due to caries at margins, filling fracture, fracture of the tooth, poor quality of the surface, leaking margin, etc.) or extensive primary caries
  • The occlusal area of the restoration must cover at least 1/3 of the occlusal area of the tooth.
  • Participant wishes a restoration within the scope of the study (signed informed consent after detailed explanation and study of the patient information)
  • 2-operative discomfort of the tooth to be restored should not exceed 3 on the visual analogue scale (VAS) (0=no pain, 10=maximum conceivable pain) due to temperature stimulus or bite sensitivity
  • Max. 2 restorations per participant in different quadrants.
  • Vital tooth
  • Healthy periodontium, no active periodontitis
  • Contact with adjacent teeth (at least at one side) and opposing teeth present with at least one contact point.
  • Sufficient language skills
Exclusion Criteria
  • Sufficient isolation not possible, dry working field cannot be guaranteed
  • Participants with a proven allergy to one of the ingredients of the materials used
  • Participants with proven allergy to local anaesthetics
  • High caries activity/ poor oral hygiene
  • Participants with severe systemic diseases
  • Pregnancy
  • Nonvital tooth or tooth with irreversible pulpitis
  • Indication for direct pulp capping
  • Symptoms of SARS-CoV2 infection

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Adhese Universal DCAdhese Universal DC-
Adhese UniversalAdhese Universal-
Primary Outcome Measures
NameTimeMethod
FDI 11 Postoperative Hypersensitivity After Inlay/Onlay Restoration, FDI Score 1-5Baseline (7-10 days)

assessed by tests with thermal stimuli and occlusal forces (during biting) determined by VAS (Visual Analog Scale) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

FDI 11 Postoperative Hypersensitivity After Inlay/Onlay Restorations, FDI Score 1-512 months

assessed by tests with thermal stimuli and occlusal forces (during biting) determined by VAS (Visual Analog Scale) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

Secondary Outcome Measures
NameTimeMethod
Vitality of Restored Teeth After Inlay/Onlay Restorations, FDI Score 1-512 months

assessed by a cold stimuli test on the patient teeth (cotton pellet and refrigerating spray) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

FDI 13 Fracture of Restored Teeth After Inlay/Onlay Restorations, FDI Score 1-512 months

assessed on patient teeth by checking tooth integrity (looking for enamel cracks, tooth fractures) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

FDI 5 Retention/Fracture of Restorations After Inlays/Onlays Restorations, FDI Score 1-512 months

assessed on patient teeth (checking inlays/onlays for fractures, cracks, small hairline cracks, chip fractures, material damage) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

FDI 6 Marginal Quality After Inlay/Onlay Restorations, FDI Score 1-512 months

assessed on the patient teeth (looking for marginal gaps/Fractures, checking outlines) following the FDI criteria on a scale from 1 "very good" to 5 "unacceptable"

Trial Locations

Locations (1)

Ivoclar Vivadent

🇱🇮

Schaan, Liechtenstein

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