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NCT02172664 · ClinicalTrials.gov registry record · NA
Clinical Evaluation of a Universal Adhesive in Noncarious Cervical Lesions
A NA study, sponsored by Indiana University.
- Completed
- Registry status
- NA
- Development phase
- 33
- Enrollment target
NCT02172664 is a NA study that has completed, run by Indiana University. The registered enrollment target is 33 participants.
The verdict
NCT02172664, a NA study, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- NA
- Development phase
- 33 participants
- Enrollment target
Study Summary
The purpose of this prospective clinical trial will be to evaluate the efficacy of an FDA approved and marketed universal dental adhesive formulation in adult noncarious cervical lesions using self-etch and selective etch approaches. The hypothesis is that using a selective enamel etch with this universal adhesive will enhance the restoration margin performance.
Interventions
- PROCEDURE Self etch enamel etching
- PROCEDURE selective etch protocol
- DEVICE Adhese Universal
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2014-06 |
| Est. Completion | 2018-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02172664
The ClinicalTrials.gov registry entry for NCT02172664 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Self etch enamel etching is the first listed.
NCT02172664 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02172664 about?
NCT02172664 is a clinical study titled "Clinical Evaluation of a Universal Adhesive in Noncarious Cervical Lesions". The purpose of this prospective clinical trial will be to evaluate the efficacy of an FDA approved and marketed universal dental adhesive formulation in adult noncarious cervical lesions using self-etch and selective etch approaches. The hypothesis is that using a selective enamel etch with this un...
What is the current status of trial NCT02172664?
This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2014-06. Estimated completion is 2018-05.
What interventions are being tested in trial NCT02172664?
The interventions under investigation include: Self etch enamel etching (PROCEDURE), selective etch protocol (PROCEDURE), Adhese Universal (DEVICE).
Who is sponsoring clinical trial NCT02172664?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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