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NCT05361746 · ClinicalTrials.gov registry record · NA
Scotchbond Universal Plus Compared to Scotchbond Universal With Filtek Universal Restorative to Restore Class V NCCLs
A NA study of Class V Non-carious Cervical Dental Lesions, sponsored by Solventum US.
- Active
- Registry status
- NA
- Development phase
- 38
- Enrollment target
- 1
- Study location
NCT05361746 is a NA study of Class V Non-carious Cervical Dental Lesions that is active but no longer recruiting, run by Solventum US. The registered enrollment target is 38 participants. The trial reports 1 study location across 1 state.
The verdict
NCT05361746, a NA study of Class V Non-carious Cervical Dental Lesions, is active but no longer recruiting, sponsored by Solventum US.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 38 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a prospective, controlled, within-subject, randomized, single-center study comparing Scotchbond Universal Plus and Scotchbond Universal adhesives when used with Filtek restorative. The study will enroll a minimum of 46 Subjects with Class-V non-carious cervical lesion (NCCL) on a minimum of two teeth.
Conditions Studied
Interventions
- DEVICE Scotchbond Universal Plus Adhesive
- DEVICE Scotchbond Universal Adhesive
Study Locations (1)
Louisiana
- Louisiana State University HSC-Health, School of Dentistry - New Orleans
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 38 participants |
| Start Date | 2022-08-18 |
| Est. Completion | 2025-07-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05361746
The ClinicalTrials.gov registry entry for NCT05361746 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Solventum US, which has 41 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Class V Non-carious Cervical Dental Lesions appearing as the primary indexed condition, and to 2 interventions - of which Scotchbond Universal Plus Adhesive is the first listed.
NCT05361746 reports 1 study location spanning 1 distinct geographic area - top geographies include Louisiana.
Frequently Asked Questions
What is clinical trial NCT05361746 about?
NCT05361746 is a clinical study titled "Scotchbond Universal Plus Compared to Scotchbond Universal With Filtek Universal Restorative to Restore Class V NCCLs". This is a prospective, controlled, within-subject, randomized, single-center study comparing Scotchbond Universal Plus and Scotchbond Universal adhesives when used with Filtek restorative. The study will enroll a minimum of 46 Subjects with Class-V non-carious cervical lesion (NCCL) on a minimum of ...
What is the current status of trial NCT05361746?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 38 participants. The study started on 2022-08-18. Estimated completion is 2025-07-30.
What conditions does trial NCT05361746 study?
This clinical trial studies the following conditions: Class V Non-carious Cervical Dental Lesions.
What interventions are being tested in trial NCT05361746?
The interventions under investigation include: Scotchbond Universal Plus Adhesive (DEVICE), Scotchbond Universal Adhesive (DEVICE).
Who is sponsoring clinical trial NCT05361746?
This trial is sponsored by Solventum US, which has 41 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05361746 being conducted?
This trial has 1 study location across Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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