Clinical trial of sodium selenite in patient with selenium deficiency
Not Applicable
- Conditions
- selenium deficiency
- Registration Number
- JPRN-UMIN000027883
- Lead Sponsor
- Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 2
Inclusion Criteria
Not provided
Exclusion Criteria
1.patients allergy to sodium selenite 2.outpatients unable to communicate with others at emergency.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method improvement of visual and sensory disturbance at 4 weeks after sodium selenite was started
- Secondary Outcome Measures
Name Time Method improvement of low serum selenium concentration at 4 weeks