Trial Information
A Study of the Association of Sleep Dysfunction and Burning Mouth Syndrome
Inclusion Criteria:
- Cases will comprise of patients diagnosed with burning mouth syndrome at the UCSF
oral medicine clinic.
- Controls will include patients with leukoplakia, pigmented lesions, traumatic
lesions, aphthous ulcers, reticular oral lichen planus, benign tumors, mucoceles, and
pemphigoid matched on age (5 years) and gender to the cases.
- New patients as well as those presenting for follow-up visits will be eligible.
Exclusion Criteria:
- Age below 18 years
- Pregnancy
- Systemic corticosteroid therapy within the previous 2 weeks.
Type of Study:
Observational
Study Design:
Observational Model: Case Control
Outcome Measure:
Sleep quality and quantity
Safety Issue:
No
Principal Investigator
Nita Chainani-Wu, DMD, MS, PhD
Investigator Role:
Principal Investigator
Investigator Affiliation:
University of California, San Francisco
Authority:
United States: Institutional Review Board
Study ID:
H1113-29221
NCT ID:
NCT00862576
Start Date:
June 2006
Completion Date:
June 2008
Related Keywords:
- Burning Mouth Syndrome
- Burning Mouth Syndrome
- Sleep
- Neuropathic pain
- Glossodynia
- Chronic pain
- Orofacial pain
- Burning Mouth Syndrome
- Burns
Name | Location |
University of California |
San Francisco, California 94108 |