Effect of Gabapentin and Hydroxyzine in pruritus of dialysis patients
Phase 2
Recruiting
- Conditions
- Pruritus.Pruritus
- Registration Number
- IRCT20160318027097N7
- Lead Sponsor
- Ardabil University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Dialysis patients; pruritus.
Exclusion Criteria
Severe dry skin; Scabies; Psoriasis; Skin lymphoma; Liver cholestasis; Neurological patients; Psychologic patients.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pruritus. Timepoint: At the beginning of the first intervention, 6 weeks after the first intervention, at the beginning of the second intervention and 6 weeks after the second intervention. Method of measurement: Pruritus Scale questionnaire.
- Secondary Outcome Measures
Name Time Method