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Chemotherapeutic Products for the Control of Gingivitis - American ...

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<strong>Chemo<strong>the</strong>rapeutic</strong> <strong>Products</strong> <strong>for</strong> <strong>Control</strong> <strong>of</strong> <strong>Gingivitis</strong>, July 2008<br />

<strong>Chemo<strong>the</strong>rapeutic</strong> <strong>Products</strong><br />

Council on Scientific Affairs <strong>for</strong> <strong>Control</strong> <strong>of</strong> <strong>Gingivitis</strong><br />

Scope: These guidelines apply to products used <strong>for</strong> <strong>the</strong> control <strong>of</strong> gingivitis and, if applicable,<br />

supragingival dental plaque, through <strong>the</strong> use <strong>of</strong> chemo<strong>the</strong>rapeutic agents. <strong>Products</strong> that control<br />

gingivitis solely by <strong>the</strong> mechanical removal <strong>of</strong> plaque will not be considered by <strong>the</strong>se guidelines.<br />

Examples <strong>of</strong> products evaluated under <strong>the</strong>se guidelines include mouthrinses and dentifrices<br />

containing agents that would destroy, inhibit or modify plaque, including its pathogenicity <strong>for</strong><br />

gingivitis, and microbiologic growth in general, those that modify <strong>the</strong> attachment <strong>of</strong> plaque<br />

microorganisms to <strong>the</strong>ir natural sites, and those that act by o<strong>the</strong>r antimicrobial mechanisms to<br />

reduce or prevent gingivitis. All studies conducted to determine ADA Acceptance <strong>of</strong> a particular<br />

product or agent should be registered with <strong>the</strong> ADA in advance, and <strong>the</strong> results <strong>of</strong> all studies<br />

must be reported, with <strong>the</strong> two considered pivotal being properly identified.

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