Efficacy and tolerability of paroxetine in patients with burning mouth syndrome
Not Applicable
- Conditions
- burning mouth syndrome
- Registration Number
- JPRN-UMIN000003266
- Lead Sponsor
- Oral Diagnosis and Medicine, Graduate Schoolof Dental Medicine, Hokkaido University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with clinically significant renal, hepatic cardiovascular diseases. Subjects taking psychotropic drugs or antidepressant within the past four weeks Abnormal hematologic examination finding Candidiasis. Pregnancy, nursing.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The cumulative proportion of responders after 12 weeks of medication. The incidence of adverse reaction during 12 weeks.
- Secondary Outcome Measures
Name Time Method