Cross-sectional Study to Assess Prevalence and Burden of CKD-associated Pruritus in Haemodialysis Patients

NCT05524467 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3100

Last updated 2024-07-09

No results posted yet for this study

Summary

Vifor International Inc. is seeking real-world evidence (RWE) to better understand the epidemiology, patient characteristics, and management of CKD-aP in the real-world clinical setting.

Conditions

  • Chronic Kidney Disease-associated Pruritus

Sponsors & Collaborators

  • Vifor (International) Inc.

    lead INDUSTRY

Principal Investigators

  • James Burton, Prof. · University of Leicester Leicester, United Kingdom

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-02
Primary Completion
2024-01-31
Completion
2024-01-31

Countries

  • Germany
  • Italy
  • Portugal
  • Spain
  • Sweden
  • Switzerland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05524467 on ClinicalTrials.gov