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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04195802
Other study ID # 69HCL69_0458
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 11, 2019
Est. completion date July 15, 2020

Study information

Verified date September 2020
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to create a self-questionnaire to evaluate sodium and potassium diet in chronic kidney disease patients.

Questionnaires will be compared to 24h sodium and potassium urinary excretion (reference) A Bayesian network and a multiple regression will be used to select the most relevant items


Recruitment information / eligibility

Status Completed
Enrollment 542
Est. completion date July 15, 2020
Est. primary completion date July 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult consulting in nephrology and having a 24h sodium urinary excretion routinely determined

- Consent informed agreement

Exclusion Criteria:

- Do not want to participate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Salt and potassium Diet
Self-administration questionnary to evaluate the salt and potassium consumption

Locations

Country Name City State
France Hôpital Edouard Herriot - Service de néphrologie - HTA - Dialyse Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The aim of the study is to create a self-administered questionnaire to evaluate sodium and potassium consumption in chronic kidney disease patients. comparison of answers to the self-questionnaire about salt and potassium diet with natriuresis and kaliuresis urinary excretion during 24 hours at inclusion