Scotchbond Universal Plus Compared to Scotchbond Universal With Filtek Universal Restorative to Restore Class V NCCLs

Completed · Not applicable

Conditions studied: Class V Non-carious Cervical Dental Lesions

In brief

This is a prospective, controlled, within-subject, randomized, single-center study comparing Scotchbond Universal Plus (SBU+) and Scotchbond Universal (SBU) adhesives when used with Filtek restorative. The study will enroll Subjects scheduled to undergo Class-V non-carious cervical lesion (NCCL) restorations.

Key facts

Study ID

NCT05361746

Run by

Solventum US LLC

People needed

38

Starts

2022-08-18

Expected to finish

2025-09-11

Last updated by the study team

2026-04-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects may be included that meet the following criteria:
• Subject is at least 18 years of age at the time of consent
• Subject is able to provide their own informed consent
• Subject has a minimum of two teeth that:
• have non-carious Class V lesions that are at least 1.5 mm deep
• are not devitalized
• have not undergone root canal treatment
• Subject has an Approximal Plaque Index score ≤ 40% as assessed via explorer and without the use of plaque-disclosing agents
• Subject is able and willing to return for all scheduled study visits
• Subject meets the Level-I or Level-II classification criteria of the American Society of Anesthesiologists (ASA) Physical Status Classification System For Dental Patient Care

You may not qualify if…

• Subjects may not be included that meet any of the following criteria:
• Subject has any of the following:
• rampant caries
• chronic periodontitis
• salivary gland dysfunction
• Subject is unable, for any reason, to tolerate the procedure time required to place the restorations
• Subject has unacceptable oral hygiene (eg, chronic moderate to heavy plaque accumulation along the gumline)
• Subject has known sensitivity to the study product components (ie, acrylate)
• Subject is planned to be enrolled in another investigational trial that requires additional interventions at any time during the study

Where it is running

• Louisiana State University HSC-Health, School of Dentistry — New Orleans, Louisiana, United States

Full record on ClinicalTrials.gov

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