A study to evaluate the efficacy of L-carnitine injection in dialysis patients with complications
Not Applicable
- Conditions
- chronic kidney disease
- Registration Number
- JPRN-UMIN000011313
- Lead Sponsor
- Showa University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients known to have a history or complication of allergy to L-carnitine. Women who are pregnant or possibly pregnant. Patients who are judged to be inappropriate to this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method sage dose of ESA
- Secondary Outcome Measures
Name Time Method serum carnitine concentration, QOL, muscle symptoms, inflammatory marker, nutritional status, cardiothoracic ratio, adverse events