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Chinese Chronic Renal Insufficiency Study: Based on Smartphone Platform (C-CRISS)

L

Limeng Chen

Status

Unknown

Conditions

Chronic Kidney Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT04229485
C-CRISS

Details and patient eligibility

About

This is a multi-center prospective cohort study. The purpose of this study is to investigate the relationship between bone metabolic markers and other non-traditional risk factors with kidney function progression, cardiovascular and cerebrovascular diseases, and bone loss in patients with CKD G3-5ND. In the meantime, this study is to explore a new mode of management and complication monitoring through mobile communication in chronic kidney disease patients.

Full description

Abnormal mineral bone metabolism of chronic kidney disease (CKD-MBD) is the most common complication of CKD. It involves kidney, bone metabolism, parathyroid gland, cardiovascular and cerebrovascular organs. It is an independent risk factor for progression of CKD to end-stage renal disease (ESRD), vascular and cardiac valve calcification, and cardiovascular and cerebrovascular events. However, less data concerning the relationship between bone metabolic index, such as high blood phosphorus and cardiovascular diseases, bone mass reduction and fracture is available in Chinese adult patients. This study is a multi-center prospective cohort study to explore the relationship between bone metabolic markers and other non-traditional risk factors with renal function progression, cardiovascular and cerebrovascular diseases, and bone loss in patients with CKD G3-5ND. Based on the sample size estimation, 3360 subjects should be enrolled in this study. The primary outcome is progression to ESRD (start dialysis or kidney transplantation) or doubling of serum creatinine, as well as cardiovascular events and all-cause mortality.

At present, the follow-up and the management of complications of CKD patients are not enough. The popularity of mobile communication in China provide the possibility to strengthen the follow-up and complications management in CKD patients and save human resources. This study is to explore a new mode of collecting datas through mobile communication in chronic kidney disease patients.

Enrollment

3,360 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • at least two measurements of serum Cr (with a minimum interval of 3 months), , 10≤eGFR≤60ml/min/1.73m^2

Exclusion criteria

  • Unable or unwilling to provide informed consent
  • Patients attending oncology, psychiatry, human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS), viral hepatitis (HBV or HCV) services
  • Acute mycardial infarction within the last six months
  • NYHA Class III or IV heart failure at baseline
  • Ongoing chemotherapy or immunosuppressive therapy (in the preceding 6 months to treat renal or immune disease)
  • Current renal replacement therapy
  • Current pregnancy or breastfeeding women
  • Any organ transplantation
  • Currently participation in an interventional clinical trial

Trial contacts and locations

1

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Central trial contact

Xuehan Zhang, MD; Xiaohong Fan, MD

Data sourced from clinicaltrials.gov

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