IRCT20180807040729N1RecruitingPhase 3
Evaluation of the effect of increased blood flow velocity compared with administration of activated charcoal suspension on severity of uremic pruritus in hemodialysis patients
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- no limit to no limit (—)
- Sex
- All
Inclusion Criteria
- •Be alert to the time, place, and individuals when collecting information
- •At least one month of uremic proritus
- •Patient diagnosed with chronic renal failure
- •Under hemodialysis for at least 6 months
- •Perform hemodialysis three times a week for at least three hours
- •Proper vascular access
- •Determine the patient's dry weight
Exclusion Criteria
- •There is a skin rash causing itching
- •The presence of liver and biliary disease
- •Unwillingness to cooperate at each stage of the research
- •Blood pressure less than 60/100 mm Hg
- •Malnutrition or any digestive problem
Investigators
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