<?xml version="1.0"?>
<Articles JournalTitle="Frontiers in Dentistry">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Frontiers in Dentistry</JournalTitle>
      <Issn>2676-296X</Issn>
      <Volume>3</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2006</Year>
        <Month>09</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of the Effect of a Clobetasol Propionate and Nystatin Mouthwash on Recurrent Aphthous Stomataitis</title>
    <FirstPage>117</FirstPage>
    <LastPage>121</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>A. Darbandi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>A. Ganbari</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Statement of problem: Recurrent aphthous stomatitis (RAS) is one of the most common diseases affecting human oral mucosa. The etiology of this disease remains unclear; therefore a definitive treatment has not yet been established and corticosteroids might be prescribed to reduce the symptoms associated with RAS.
Purpose: The aim of this study was to determine the effects of a mouthwash containing 0.05% clobetasol and nystatin on aphthous ulcers.
Materials and Methods: Forty patients with RAS, 18 males and 22 females with an age range of 11-50 years, participated in this double-blind placebo-controlled clinical trial. The subjects were randomly divided into two equal groups. Group A received a mouthwash containing 0.05% clobetasol and 100,000 IU/cc nystatin with instructions to rinse with 20 drops for 5 minutes, 3 times daily. Group B (control) received placebo and was asked to follow the same instructions. All symptoms along with possible adverse effects were measured and recorded during the 2-week study period. Statistical analysis was performed using chi-square and independent paired t-tests. 
Results: Complete resolution of the lesions and their symptoms was observed in 85% of the participants in group A. Two (10%) patients showed no response to treatment and the symptoms increased in 5% (1 patient). There were no measurable changes in pain or healing time of the ulcers in the control group.
Conclusion: The use of the tested mouthwash was found to be a safe and efficacious treatment for RAS of the oral mucosa.</abstract>
    <web_url>https://fid.tums.ac.ir/index.php/fid/article/view/92</web_url>
    <pdf_url>https://fid.tums.ac.ir/index.php/fid/article/download/92/92</pdf_url>
  </Article>
</Articles>
