Actively Recruiting

Age: 18Years +
All Genders
ID02989298

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients receiving peritoneal dialysis treatment
  • Adults aged 18 years and older
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surveillance

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

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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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