Actively Recruiting
Peritoneal Dialysis Registration System (PERSIST) for End Stage Renal Disease Patients
Led by Sun Yat-sen University · Updated on 2020-10-22
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are creating a database by registering all patients with end stage renal disease (ESRD) receiving peritoneal dialysis (PD) treatment at selected hospitals in China. This observational study aims to collect and analyze detailed demographic, clinical, and treatment data to better understand long-term outcomes for PD patients, including survival, complications, and quality of life. Patients' baseline information such as age, gender, height, weight, smoking and drinking habits, education, primary cause of ESRD, dialysis prescriptions, clinical lab results, drug use, and complications will be collected. Participants will be followed every three months to update clinical data, complications, drug information, and quality of life scores. The study will track outcomes like patient survival, technique survival, peritonitis rates, hospitalizations, kidney transplantation, and transfers to hemodialysis up to 10 years. During the study, patients will undergo regular follow-ups every three months where demographic and clinical data, lab results, and quality of life measurements will be gathered and entered into the registry system. The research team will analyze trends in patient survival, technical survival of PD, changes in kidney and peritoneal function, and complication rates over time. This long-term registry will provide valuable insights into PD patient outcomes and treatment effectiveness.
CONDITIONS
Brief Title
Peritoneal Dialysis Registration System (PERSIST)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients receiving peritoneal dialysis treatment
- Adults aged 18 years and older
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 10 years
Participants who undergo routine peritoneal dialysis care are observed. Demographic and clinical characteristics, complications, drug information, and quality of life scores are collected at baseline and during follow-up visits.
Visits every 3 months
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China, 510080
Actively Recruiting
Research Team
X
Xueqing Yu, M.D. & Ph.D.
X
Xiao Yang, M.D. & Ph.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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