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Evaluation of the effect of Zinc Sulfate on pruritus in patients under hemodialysis

Not Applicable
Conditions
Pruritus in Hemodialysis Patients.
End-stage renal disease
Registration Number
IRCT138806082370N2
Lead Sponsor
Vice Chancellor for Research, School of Medicine, Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

- Being under maintenance hemodialysis for at least one month
- Not being under other drug treatment for pruritus
- Having pruritus for at least 8 wk
- No sensitivity to Zinc Sulfate
- Volunteer to participate
Exclusion criteria:
- Non compliance with drug
- Renal transplantation before end of therapy
- Hypoparathyroidism
- Alkalin phosphatase elevation

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in Pruritus Score. Timepoint: Every 2 wk. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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