Salivary Catecholamines in Aphthous Stomatitis (Canker Sores)

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2006-08-31

Study Completion Date

2009-12-31

Brief Summary

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The purpose of this study is to examine how compounds produced in patients with canker sores affect wound healing.

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Detailed Description

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The purpose of this study is to determine if salivary catecholamines are elevated in patients with the disease aphthous stomatitis. The results of this study will be combined with those performed in collaboration with a co-Investigator to understand the effects of catecholamines on mucosal wound healing and oral epithelial cell migration.

Conditions

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Canker Sore

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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1

Individuals with a history of canker sores.

No interventions assigned to this group

2

Individuals with no history of canker sores.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age 18 or older, both genders
* History of recurrent aphthous ulcers with 4 or more episodes per year

Exclusion Criteria

* History of salivary gland disease including Sjogren's disease, parotitis, and sialolithiasis
* History of benign or malignant salivary gland tumor
* History of celiac disease, ulcerative colitis or Crohn's disease
* Patients on medications that affect salivary flow such as anti-depressants and anti-cholinergic medications

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes