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Clinical Evaluation of Three Dental Adhesive Systems in Class V Restorations

Clinical Evaluation of Three Dental Adhesive Systems in Class V Restorations

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00643461
Enrollment
46
Registered
2008-03-26
Start date
2008-04-30
Completion date
2012-06-30
Last updated
2024-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries

Brief summary

The purpose of this study is to compare the clinical performance of three dental adhesive systems used to bond Class V cavity fillings in adult teeth.

Interventions

DEVICEAdhesive A

Applied per manufacturer's instructions.

DEVICEAdhesive B

Applied per manufacturer's instructions.

DEVICEAdhesive C

Applied per manufacturer's instructions.

Sponsors

3M
CollaboratorINDUSTRY
Solventum US LLC
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Must be at least 19 years of age * Must have at least 3 qualifying noncarious Class V lesions of appropriate depth * Must be willing to sign consent form * Must be willing and able to return to UAB clinic for 4 study appointments * Must be in good medical health and able to tolerate dental procedures

Exclusion criteria

* Current participation in other restorative product studies * Severe salivary gland dysfunction * Rampant caries (cavities) * Chronic periodontitis (gum disease) * Known allergies to the study materials * Unacceptable level of oral hygiene * Inability or unwillingness to attend study appointments

Design outcomes

Primary

MeasureTime frame
Retention of the restoration.6, 12, 24, 36 months post-placement

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026