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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00556686
Other study ID # 200614581
Secondary ID
Status Withdrawn
Phase N/A
First received November 8, 2007
Last updated April 20, 2015
Start date August 2006
Est. completion date December 2009

Study information

Verified date April 2015
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of California, Davis
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04914533 - Luminance RED for Canker Sores N/A