Kidney AI-enabled Care Transformation

NCT05056909 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2023-02-02

No results posted yet for this study

Summary

In the Kidney ACTion study, CKD (Chronic Kidney Disease) patients at increased risk of progression to ESRD (End Stage Renal Disease) will be randomly assigned to either standard of care in a specialist nephrology outpatient clinic or to receiving CKD care supported by a novel AI-supported (Artificial Intelligence) software solution.

Conditions

  • Chronic Kidney Diseases

Interventions

DEVICE

Kidney ACTion

AI-supported software for chronic kidney disease care

OTHER

Standard of care

Standard of care

Sponsors & Collaborators

  • Fraunhofer Institut für Arbeitswirtschaft und Organisation

    collaborator UNKNOWN
  • Empirica

    collaborator UNKNOWN
  • IN-JET APS

    collaborator UNKNOWN
  • CNET Svenska AB

    collaborator UNKNOWN
  • XIGME

    collaborator UNKNOWN
  • European ESKD Patients' Federation

    collaborator UNKNOWN
  • Catholic University of the Sacred Heart

    collaborator OTHER
  • University of Manchester

    collaborator OTHER
  • Università degli studi di Verona

    collaborator UNKNOWN
  • University of Leeds

    collaborator OTHER
  • Roche Diagnostics International AG

    collaborator INDUSTRY
  • Federación Nacional ALCER

    collaborator UNKNOWN
  • Medical University of Graz

    lead OTHER

Principal Investigators

  • Alexander H Kirsch, MD · Medical University of Graz

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-30
Primary Completion
2024-05-31
Completion
2024-10-31

Countries

  • Italy
  • United Kingdom

Study Locations

More Related Trials

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 NCT05056909 on ClinicalTrials.gov