Exploratory clinical trial of dialysis dose monitor with optical measurement
Not Applicable
- Conditions
- End stage renal disease
- Registration Number
- JPRN-UMIN000011082
- Lead Sponsor
- Tokyo Women's Medical University Department of Blood Purification
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
Severe hypertension over systolic pressure of 120 mmHg Significant recirculation of blood access Pregnat patients, suspected of being pregnant or lactating patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Correlation with urea concentration of dialysis effluent and blood by the dialysis dose monitor
- Secondary Outcome Measures
Name Time Method