About this trial
Brief Summary: The investigators are registering all PD patients at recruited hospitals and developing a PD database in China. Patients will be followed up every 3 months, and both baseline and follow-up information will be collected and input into the registration system. The patient survival, technical survival, peritonitis rate, longitudinal changes of residual renal function and peritoneum function, and quality of life for PD patients, etc, will be compared using the PD database.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
ESRD patients receiving PD treatment
Trial design
Cohort
Prospective
Treatments tested in this trial
No intervention
Other interventionRegistration of all PD 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
Patient survival of PD patients
Patient survival including all-cause and cardiovascular mortality.
Secondary outcomes
Technical survival of PD patients
Sponsors and contacts
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