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Clinical Trial Summary

The aim of this study is to evaluate the effects and efficacy of dietary sodium restriction by mean of a new healthcare approach in patients with immunoglobulin A nephropathy. The test persons in the intervention group are actively supported to adhere to a restricted sodium diet with a structured education program in combination with regular sodium excretion monitoring.


Clinical Trial Description

Patients in the intervention group receive regular sodium-restriction education by a dietician, which entails introducing food types and cooking skills, quantifying salt intake with a special spoon and recording detailed interactive food diary. Sodium excretion was measured using one 24-hour urine collection regularly to assess dietary compliance and enable feedback. The test persons with sodium excretion higher than 90mmol/24h will receive intensive education. Test persons in the control group receive standard care. After 2 weeks in study, all test persons visit the outpatient clinic for measurements and data collection. Within 3 months of total study duration, data collection and measurements take place at the end of every month. At each timepoint blood and 24-hourly urine is collected, test persons fill out questionnaires. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04805047
Study type Interventional
Source First Affiliated Hospital Xi'an Jiaotong University
Contact Huixian Li
Phone 17792905602
Email lihuixian_muye@163.com
Status Recruiting
Phase N/A
Start date May 15, 2021
Completion date December 2023

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