About this trial
The investigators are registering all HD patients at recruited hospitals and developing a HD database in China. Patients will be follow-up every 3 months, and both baseline and follow-up information will be entered into the registration system. The patient survival, technical survival, patency rate of access, quality of life and residual renal function for HD patients will be compared using the HD database.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
End stage renal disease patients receiving hemodialysis treatment
Trial design
Cohort
Prospective
Treatments tested in this trial
No intervention
Other interventionRegistration of all HD patients in the First Affiliated Hospital of Sun Yat-sen University and other hospital which have signed the contract in China.
Treatment groups
Trial outcomes
Primary outcomes
Patient survival of HD patients
Secondary outcomes
Quality of life evaluated using SF36 scale for HD patients
Patency rate of access for HD patients
Sponsors and contacts
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