External Validation of Clinical Prediction Tools for Estimating Salt and Potassium Intake in Nephrology Patients.
NCT ID: NCT05783960
Last Updated: 2024-11-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
629 participants
OBSERVATIONAL
2023-07-16
2024-07-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Using Bayesian models, researchers developed clinical prediction tools to estimate salt and potassium intake in nephrology patients. These prediction tools performed well, with an accuracy of 89% for salt and 74% for potassium, and have undergone internal validation.
Currently, the investigators wish to conduct an external validation study of these clinical prediction tools using data from patients followed at 3 nephrologic centers to generalize the performance results of the tools.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Self-administered Questionnaire to Evaluate Salt and Potassium Diet of Patients Followed in Nephrology
NCT04195802
Nurse-Led Nutritional Education for Moroccan Dialysis Patients
NCT07277530
CENtral Blood Pressure Targeting: a Pragmatic RAndomized Pilot TriaL in Advanced Chronic Kidney Disease
NCT05163158
Renin Angiotensin Aldosterone System In Septic Kids
NCT06295393
Validation of Renal Perfusion CEUS Against MRI, and Its Application in Acute Kidney Injury
NCT04181281
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
External validation a questionnaire
Questionnaire will be administrated to patient with chronic kidney diseases ti evaluated the consumption of salt and potassium intake. A Bayesian network and a multiple regression will be used to validated the questionary of 27 items
administration questionary
Questionnaire will be compared to 24h sodium and potassium urinary excretion (reference). A Bayesian network and a multiple regression will be used to validate the questionary
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
administration questionary
Questionnaire will be compared to 24h sodium and potassium urinary excretion (reference). A Bayesian network and a multiple regression will be used to validate the questionary
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Consultant or inpatient in the nephrology department
* Having performed a 24-hour urinary assessment as part of his usual management with analysis of natriuresis and/or kaliuresis.
Exclusion Criteria
* Person protected by the french law
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hospices Civils de Lyon
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jean Pierre Fauvel
Role: PRINCIPAL_INVESTIGATOR
Service Nephrologie, Hôpital Edouard Herriot
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Service de néphrologie Hôpitaux Universitaires de Strasbourg
Strasbourg, Alsace, France
AURAL
Lyon, , France
Hopital Lyon SUD
Lyon, , France
HÖPITAL bichat
Paris, , France
CHU Rangueil
Toulouse, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
69HCL23_0239
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.