Peritoneal Dialysis Registration System (PERSIST)

NCT ID: NCT02989298

Last Updated: 2020-10-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-31

Study Completion Date

2026-12-31

Brief Summary

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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.

Detailed Description

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Detailed Description: The investigators are registering all end stage renal disease (ESRD) patients receiving peritoneal dialysis (PD) treatment, and developing a PD database in China. Patients' demographic characteristics (including age, gender, height, weight, BMI, smoking, drinking, and education, etc), clinical characteristics (primary cause of ESRD, dialysis prescription, patient's condition and lab measurements of serum, urine, and dialysate), drug information, complications and scores of quality of life at the baseline will be collected. Patients will be followed up every 3 months. Demographic and clinical characteristics, complications, drug information of patients will be collected at each visit. The patients' clinical outcomes, such as mortality (including all-cause mortality and cardiovascular disease mortality), technical survival, kidney transplantation, transfer to hemodialysis, hospitalization, occurrence of peritonitis, etc. were also followed up till the end of the study. The data of patient survival, technical survival, peritonitis rate, hospitalization rate, clinical lab parameters, longitudinal changes of residual renal function and peritoneum function, peritonitis rate, hospitalization rate, clinical lab parameters and quality of life for PD patients will be analyzed using the PD database.

Conditions

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ESRD Disorders Associated With Peritoneal Dialysis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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PD patients

End stage renal disease patients receiving peritoneal dialysis treatment

No intervention

Intervention Type OTHER

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.

Interventions

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No intervention

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.

Intervention Type OTHER

Eligibility Criteria

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Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sun Yat-sen University

OTHER

Sponsor Role lead

Responsible Party

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Xue Qing Yu

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Xueqing Yu, M.D. & Ph.D.

Role: PRINCIPAL_INVESTIGATOR

First Affiliated Hospital, Sun Yat-Sen University

Locations

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The First Affiliated Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Xueqing Yu, M.D. & Ph.D.

Role: CONTACT

8620-87766335

Xiao Yang, M.D. & Ph.D.

Role: CONTACT

8620-87755766 ext. 8843

Facility Contacts

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Xueqing Yu, M.D. & Ph.D

Role: primary

8620-87766335

Other Identifiers

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PD registry

Identifier Type: -

Identifier Source: org_study_id

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