About this trial
The investigators are registering all nephrotic syndrome (NS) patients regardless of the primary causes and developing a NS database in China. Patients will be followed-up and both baseline and follow-up information will be recorded in the registration system. The treatment response, longitudinal changes of renal function, renal survival, patient survival, infection events and acute kidney injury etc, will be analyzed using the NS database.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Nephrotic syndrome patients regardless of the primary causes
Disqualifiers
No
Trial population
Nephrotic syndrome patients
Trial design
Cohort
Prospective
Treatments tested in this trial
No intervention
Other interventionRegistration of all NS patients in the First Affiliated Hospital of Sun Yat-sen University and other hospitals which have signed the contract in China.
Treatment groups
Trial outcomes
Primary outcomes
The patient survival in NS patients
Secondary outcomes
Renal survival in NS patients
Renal survival including end stage renal disease, dialysis, renal transplantation
Longitudinal changes of renal function of NS patients
Treatment response of NS patients
Infection rate of NS patients
Sponsors and contacts
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