The effect of topical piroxicam in the treatment of uremic pruritus
Phase 3
Completed
- Conditions
- remic pruritus.Pruritus
- Registration Number
- IRCT20191106045356N18
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients undergoing hemodialysis more than 3 times a month
Insensitivity to piroxicam
Patients with chronic uremic pruritus
Absence of pregnancy and breastfeeding
Exclusion Criteria
Patients with underlying skin disease
Allergic to Piroxicam
Pregnancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method remic pruritus. Timepoint: ?Before intervention and 7, 14 days after intervention. Method of measurement: Pruritus questionnaire.
- Secondary Outcome Measures
Name Time Method