ACTRN12610000741088
Completed
Phase 3
A randomized controlled clinical trial comparing the efficacy of Dead Sea mineral enriched body lotion vs. two types of placebo in the treatment of cutaneous dryness, itching, peeling and tightness in hemodialysis patients: EDIT
Ahava Dead Sea Laboratories and Dead Sea Research Center0 sites75 target enrollmentSeptember 6, 2010
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Skin - Dermatological conditions
- Sponsor
- Ahava Dead Sea Laboratories and Dead Sea Research Center
- Enrollment
- 75
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Hemodialysis (HD) patients aged 40\-80 years inclusive were eligible for study participation if they received HD treatment three times each week for not less than three months, and if they were willing to refrain from any antipruritic treatment, oral or topical, for a period of not less than two weeks prior to study initiation. Patients of both genders, without regard to comorbidities or prescribed medications, were eligible.
Exclusion Criteria
- •Patient unwillingness to participate for any reason; known sensitivity to any of the ingredients in the active or placebo treatments.
Outcomes
Primary Outcomes
Not specified
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