Peritoneal Dialysis Registration System (PERSIST)
1 other identifier
observational
10,000
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2013
CompletedFirst Submitted
Initial submission to the registry
October 17, 2016
CompletedFirst Posted
Study publicly available on registry
December 12, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
October 22, 2020
October 1, 2020
13 years
October 17, 2016
October 20, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Patient survival of PD patients
Patient survival including all-cause and cardiovascular mortality.
10 years
Secondary Outcomes (1)
Technical survival of PD patients
10 years
Study Arms (1)
PD patients
End stage renal disease patients receiving peritoneal dialysis treatment
Interventions
Registration of all PD patients in the First Affiliated Hospital of Sun Yat-sen University and other hospitals,which have signed the contract in China.
Eligibility Criteria
ESRD patients receiving PD treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, 510080, China
Biospecimen
The serum, urine, DNA and peritoneum tissue will be collected.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xueqing Yu, M.D. & Ph.D.
First Affiliated Hospital, Sun Yat-Sen University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 17, 2016
First Posted
December 12, 2016
Study Start
December 1, 2013
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
October 22, 2020
Record last verified: 2020-10