- * Male or female adult patients with CKD (≥18 years) receiving HD for at least 3 months prior to signing informed consent
- * Signed informed consent
- * Able and willing to fill in questionnaires
Chronic Kidney Disease-associated Pruritus
Cross-sectional Study to Assess Prevalence and Burden of CKD-associated Pruritus in Hemodialysis Patients
NCT05625542 | PHASE 1 | OBSERVATIONAL
Vifor International Ltd. is seeking real-world evidence (RWE) to better understand the epidemiology, patient characteristics, and management of CKD-aP in the real-world clinical setting.
Trial Information
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Study Eligibility Criteria
Additional Studies
Additional studies can be found at ClinicalTrials.gov