Actively Recruiting
A Prospecitve Multicenter, Observational Registry Study
Led by AstraZeneca · Updated on 2026-05-12
3000
Participants Needed
1
Research Sites
148 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, multicenter, observational registry study designed to collect data to deepen the understanding of CKD therapeutics, changes in clinical practice, cardiorenal risk outcomes and differences in treatment approaches in Chinese CKD patients.
CONDITIONS
Official Title
A Prospecitve Multicenter, Observational Registry Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients aged �3E= 18 years
- Willing and able to provide written informed consent to participate in the study
- Confirmed chronic kidney disease diagnosis at enrollment, defined by either:
- eGFR less than 60 mL/min/1.73 m�b2 for 3 months or more
- Evidence of kidney damage such as urine albumin-to-creatinine ratio (UACR) �3E= 30 mg/g, urine protein-to-creatinine ratio (UPCR) �3E= 150 mg/g, structural abnormalities on imaging, or kidney biopsy findings consistent with chronic kidney injury persisting for 3 months or more
You will not qualify if you...
- Life-threatening comorbidity with life expectancy less than 2 years
- Severe cardiac disease including life-threatening arrhythmias or recent major adverse cardiovascular events (MI, stroke, cardiovascular death) within the past 3 months
- Pregnant or breastfeeding women
- Currently enrolled in any interventional clinical trial or receiving investigational therapy within 3 months of enrollment
- Presenting with end-stage renal disease (ESRD), receiving renal replacement therapy (RRT), acute kidney injury (AKI), or acute kidney disease as a primary condition at enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Zhongshan Hospital Affilicated with Fudan University
Shanghai, China
Actively Recruiting
Research Team
A
AstraZeneca Clinical Study Information Center
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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