A randomised controlled trial of treatment with SSRI or SNRI for patients with functional (psychogenic) dizziness
Not Applicable
- Conditions
- functional (psychogenic) dizziness
- Registration Number
- JPRN-UMIN000031958
- Lead Sponsor
- Department of Psychosomatic Medicine, Toho University School of Medicine
- Brief Summary
Thirteen people participated, but 10 people were included in the analysis due to dropouts. As for changes after 4 weeks, CGI and VSS-sf improved in all patients in the escitalopram group, showing a statistically significant decreasing tendency. No significant changes were observed after 4 weeks in the control group and the milnacipran group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 13
Inclusion Criteria
Not provided
Exclusion Criteria
Subjects are excluded if they express suicidal ideation. Other exclusion criteria are currently undergoing treatment with antidepressants or no understanding ability of this study themselves, or no intention of participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method