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NCT01629290 · ClinicalTrials.gov registry record · NA
In Vivo Comparison of Salivary Fluoride Levels Following the Application of Different 5% NaF Varnishes
A NA study, sponsored by University of Michigan.
- Completed
- Registry status
- NA
- Development phase
- 15
- Enrollment target
NCT01629290 is a NA study that has completed, run by University of Michigan. The registered enrollment target is 15 participants.
The verdict
NCT01629290, a NA study, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
Study Summary
This study will be a cross-over single blinded clinical study to evaluate the in vitro fluoride release of three different brands of 5% NaF varnish. The goal of this study is to determine if different formulations of varnish lead to differing amounts of fluoride release. Despite their similar concentrations of NaF (5%), some in vitro data have suggested that they may differ in the amount of fluoride release. Determining fluoride release of these varnishes in vivo is important in assessing both the safety and efficacy of the product.
Interventions
- DEVICE Placebo
- DEVICE Enamel Pro
- DEVICE Duraphat
- DEVICE Vanish
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2012-06 |
| Est. Completion | 2015-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01629290
The ClinicalTrials.gov registry entry for NCT01629290 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.
NCT01629290 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01629290 about?
NCT01629290 is a clinical study titled "In Vivo Comparison of Salivary Fluoride Levels Following the Application of Different 5% NaF Varnishes". This study will be a cross-over single blinded clinical study to evaluate the in vitro fluoride release of three different brands of 5% NaF varnish. The goal of this study is to determine if different formulations of varnish lead to differing amounts of fluoride release. Despite their similar concen...
What is the current status of trial NCT01629290?
This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2012-06. Estimated completion is 2015-12.
What interventions are being tested in trial NCT01629290?
The interventions under investigation include: Placebo (DEVICE), Enamel Pro (DEVICE), Duraphat (DEVICE), Vanish (DEVICE).
Who is sponsoring clinical trial NCT01629290?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
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