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Clinical Trials/IRCT20180807040729N1
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

Shahroud University of Medical Sciences0 sites60 target enrollmentStarted: TBDLast updated:

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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