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Tokushima Night Guard for Recurrent Aphthous Stomatitis

NCT02890524 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2019-04-17

No results posted yet for this study

Summary

The investigators will investigate whether the night guard can suppress the development of recurrent aphthous stomatitis (RAS). The investigators will record the patients' oral condition for 60 days before and after intervention with the night guard made of Ethylene-Vinyl Acetate copolymer (EVA). The patients' saliva will be analyzed for measurement of inflammatory cytokines or oxidative stress.

Conditions

  • Aphthous Stomatitis

Interventions

DEVICE

night guard

60 days before and after intervention with the night guard

DEVICE

placebo night guard

60 days before and after intervention with the placebo night guard

Sponsors & Collaborators

  • University of Tokushima

    lead OTHER

Principal Investigators

  • Yasusei Kudo, DDS, PhD · Tokushima University

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2018-03-31
Completion
2018-03-31

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02890524 on ClinicalTrials.gov