KCT0009036
Not yet recruiting
未知
Efficacy and Safety Evaluation of Hemoglobin Control by Erythrocyte Stimulate Agent Recommendation Algorithm in Kidney Failure with Renal Replacement Therapy: Multicenter, Prospective, Single Blind, Randomization Control Trials
ConditionsDiseases of the genitourinary system
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the genitourinary system
- Sponsor
- Yonsei University Health System, Severance Hospital
- Enrollment
- 250
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with end\-stage renal disease who have been on hemodialysis for more than 6 months
- •\- Patients with hemoglobin levels above 8\.0 g/dL and below 14\.0 g/dL
- •\- Patients using or planning to use Darbepoetin alpha
- •\- Adults over 19 years old and under 80 years old
- •\- Patients weighing more than 40\.0 kg and less than 100\.0 kg
- •\- Among the target subjects, patients whose voluntary consent procedure was confirmed after explanation of the clinical trial
- •\- Patients who can collect clinical variables for the past 5 months from the time of study registration required for algorithm operation
Exclusion Criteria
- •\- Patients temporarily receiving hemodialysis due to acute kidney disease
- •\- Patients temporarily undergoing hemodialysis before transplantation
- •\- Patients who have experienced blood transfusion within 3 months of participating in the study
- •\- Patients with serious systemic condition
- •\- Patients with low compliance, e.g., people with mental illness
- •\- Patients withdrew from clinical trials
Outcomes
Primary Outcomes
Not specified
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