comparative study on the increase of blood flow velocity and administration of oral activated charcoal on the severity of uremic pruritus in hemodialysis patients

Phase 3

Recruiting

• Conditions: remic pruritus in hemodialysis patients.; Other pruritus

• Registration Number: IRCT20180807040729N1
• Lead Sponsor: Shahroud University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The incidence of itching according to the score of the questionnaire Yosipovich. Timepoint: The questionnaire will be completed in six steps:1- Before intervention in each group 2- Immediately after the first intervention in a triple group (first period) 3- After the first wash out in the first period 4- Immediately after the interventions defined in the second period 5. After the second wash out 6. Immediately after the interventions defined in the third period. Method of measurement: The severity of itching will be measured using the Yosipovich questionnaire.