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Prognostic Value of a Multidimensional Assessment for Survival in Elderly Patients With CKD 4B/5 (PROFILER)

C

Centre Hospitalier Universitaire de Besancon

Status

Not yet enrolling

Conditions

Chronic Kidney Disease Stage 4B
Chronic Kidney Disease Stage 5

Study type

Observational

Funder types

Other

Identifiers

NCT06825234
2024/912

Details and patient eligibility

About

The aim of this study is to determine a multidimensional signature (integrating frailty and patient-reported outcomes measures (PROMs) at entry into stage 4B/5 CKD) to improve prediction of renal death (dialysis, transplantation, conservative management, death).

Full description

In 2019, 4,263 patients starting dialysis in France were aged 75 years or older. This elderly population, often with comorbidities, poses a number of challenges for nephrologists, both in terms of initiation and modalities of dialysis and access to transplantation. Dialysis may offer little benefit in terms of survival, often at the cost of a significant impact on quality of life and number of hospitalisations. There is a current trend to offer conservative treatment as an alternative to dialysis. However, there are no objective criteria to guide this decision and the uremic syndrome may distort certain clinical perceptions. The aim of this study is to determine whether an assessment that incorporates multiple dimensions, including those of frailty, can help the clinician determine the best course of treatment for the patient.

Enrollment

390 estimated patients

Sex

All

Ages

75+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with CKD stage 4B or 5 (first consultation with GFR < 20 mL/min /1.73 m2 in CKD-EPI 2009).
  • Fluency in French
  • Membership of a French social security scheme
  • Non-opposition from the subject to participate in the study

Exclusion criteria

  • Subjects with limited legal capacity.
  • Subjects still in the exclusion period of another study, or according to the national registry of clinical trial participants.
  • Subjects with no social security coverage.
  • Subjects judged by the investigator to be unlikely to comply with study procedures
  • Subjects unable to understand the reasons for the study; psychiatric disorders judged by the investigator to be incompatible with inclusion in the study.

Trial contacts and locations

2

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Central trial contact

Charline Vauchy, PhD.

Data sourced from clinicaltrials.gov

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