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Recruiting

NCT Number: NCT03001921

Wise Practice of Chinese Hemodialysis (WISHES)

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The 1st Affiliated Hospital, Sun Yet-sen University

Guangzhou, Guangdong, 510080, China

Location status: Recruiting

Location contact

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

CONTACT

[email protected]

Xueqing Yu, MD

PRINCIPAL_INVESTIGATOR

About this study

The investigators are registering all end stage renal disease (ESRD) patients receiving hemodialysis (HD) treatment, and developing a HD database in China. Patients' demographic characteristics (including age, gender, height, weight, BMI, smoking, drinking, and education), clinical characteristics (including systolic blood pressure, diastolic blood pressure, primary cause of ESRD, and lab measurements of serum, urine, and access patency), complications, drug information and scores of quality of life at the baseline will be collected. Patients will be follow-up every 3 month, the demographic and clinical characteristics, complications and drug information of patients will be collected at each visit. The investigators also record the outcome at each visit, such as mortality (including all-cause mortality and cardiovascular disease mortality), technical survival, kidney transplantation, transfer to peritoneal dialysis, hospitalization, access failure,etc. 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

End stage renal disease patients receiving hemodialysis treatment.

Exclusion criteria

No

Treatment and study plan

No intervention

Other

Registration of all HD patients in the First Affiliated Hospital of Sun Yat-sen University and other hospital which have signed the contract in China.

Primary outcomes

  1. Patient survival of HD patients

    Time frame: 10 years

Secondary outcomes

  1. Quality of life evaluated using SF36 scale for HD patients

    Time frame: 10 years

  2. Patency rate of access for HD patients

    Time frame: 10 years

Study contacts

Contact information is provided by the study sponsor or research team.

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

CONTACT

[email protected]

Xunhua Zheng, M.D. & Ph.D.

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Important dates

Study start
2013
Primary completion
2026
Study completion
2027
First posted
Dec 23, 2016
Registry last updated
Oct 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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