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

NCT ID: NCT06825234

Last Updated: 2025-05-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

390 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-30

Study Completion Date

2028-12-31

Brief Summary

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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).

Detailed Description

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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.

Conditions

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Chronic Kidney Disease Stage 5 Chronic Kidney Disease Stage 4B

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Besançon University Hospital

Besançon, , France

Site Status

Tours University Hospital

Tours, , France

Site Status

Countries

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France

Central Contacts

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Charline Vauchy, PhD.

Role: CONTACT

+33381218875

Facility Contacts

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Charline Vauchy, PhD

Role: primary

Other Identifiers

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2024/912

Identifier Type: -

Identifier Source: org_study_id

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