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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01584024
Other study ID # N010508-S3
Secondary ID 12-PAF02598
Status Completed
Phase N/A
First received
Last updated
Start date March 2013
Est. completion date December 31, 2017

Study information

Verified date January 2019
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether lesion infiltration is an effective management strategy to arrest early tooth decay.


Description:

A 3-year prospective, randomized control clinical trial (RCT) is designed incorporating a split mouth intra-oral design. Young volunteers (18-24 years old) with at least two early lesions in posterior teeth will be enrolled into this clinical trial to evaluate the clinical effectiveness of arresting lesion progression by resin infiltration therapy as adjunct to standard-of-care preventative measures. Lesion status (non-cavitated) is clinically confirmed prior to implementing the assigned therapy.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria:

- DMFT = 3 (DMFT = index of decayed-missing-filled permanent teeth)

- Having at least two early caries lesions in approximal posterior tooth surfaces

- Lesions visible on radiograph

Exclusion Criteria:

- Current participation in another clinical study

- Medically compromised subjects

- Hyposalivation

- Pregnancy

- Allergic to methylmethacrylates

- Allergic to latex

- Symptomatic teeth

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Resin infiltration
Baseline treatment of one caries lesion with resin infiltration therapy, in addition to preventative measures and behavioral modification. ICON product: FDA-510(k): K100062
Sham treatment
Baseline treatment of one caries lesion with sham treatment, in addition to preventative measures and behavioral modification.

Locations

Country Name City State
United States Saunders USADC West Point New York

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan DMG Dental Material Gesellschaft mbH

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Lesions With Progression as Measured by Pairwise (PW) Comparison (N=Lesions) Cumulative lesion progression as measured by PW comparison of radiographs (baseline versus 3 year) 3 Years
Secondary Number of Lesions With Progression as Measured by Depth Category (N=Lesions) Radiographic lesion depth categories: E2 (inner enamel), D1 (outer dentin) and D2-rest (middle dentin or restored). Lesion depth assessment on single radiograph (baseline, 3 yr). 3 Years
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