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A Controlled Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Pruritus in Adult Hemodialysis Patients
The purpose of this research study is to evaluate the efficacy of SARNA Sensitive Lotion in the treatment of uremic pruritus in adult hemodialysis patients in a double-blind Controlled comparative trial.
Details
| Lead sponsor | Wake Forest University |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 28 |
| Start date | 2006-11 |
| Completion | 2008-10 |
Conditions
- Pruritis
Interventions
- Sarna
- Cetaphil
Primary outcomes
- Investigator Global Assessment — Disease severity assessed at baseline and 4 weeks, week 4 reported
Investigator's Global Assessment Disease Severity is based on the following scale: 0 = completely clear: except for possible residual hyper pigmentation 1. = almost clear: very significant clearance (about 90%) 2. = Marked improvement: significant improvement (about 75%) 3. = Moderate improvement: intermediate between slight and marked; representing about 50% improvements 4. = Slight improvement: some improvement (about 25%); however, significant disease remaining 5. = No change (moderate to severe disease) 6. = Worse
Countries
United States