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High-Risk Chronic Kidney Disease Registry in China

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Study Aim

This study aims to observe and track changes in kidney health, heart events, and overall mortality in individuals with high-risk chronic kidney disease in China.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Urogenital Diseases+9

+ Chronic Disease

+ Female Urogenital Diseases and Pregnancy Complications

Over 18 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: November 2023
See protocol details

Summary

Principal SponsorAstraZeneca
Study ContactAstraZeneca Clinical Study Information Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 28, 2023

Actual date on which the first participant was enrolled.

Chronic Kidney Disease (CKD) is a prevalent and serious health issue known for its high treatment costs and poor awareness among patients. Many individuals with CKD experience severe symptoms such as heavy protein in their urine and uncontrolled high blood pressure, which can worsen the disease and lead to heart problems and higher chances of hospitalization and mortality. This study is important as it aims to create a registry platform focusing on high-risk CKD patients in China. By collecting detailed information about these patients, the study seeks to understand the factors that contribute to the progression of CKD and to improve future predictions and treatments. Participants in this study will include around 5,000 CKD patients from various locations in China, and the study will last from 2023 to 2027. The study will gather baseline information and continue to collect data annually on the patients' health, treatments, and outcomes. Researchers will track changes in the patients' kidney function, protein levels in urine, and any heart-related issues or hospitalizations. The goal is to identify patterns and risk factors that could lead to better treatment guidelines and prediction models for CKD patient outcomes, ultimately aiming to enhance patient care and reduce the burden of the disease.

Official TitleChronic Kidney Disease Registry Platform Study
NCT06117852
Principal SponsorAstraZeneca
Study ContactAstraZeneca Clinical Study Information Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1900 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesChronic DiseaseFemale Urogenital Diseases and Pregnancy ComplicationsKidney DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsUrologic DiseasesDisease AttributesRenal Insufficiency, ChronicRenal InsufficiencyFemale Urogenital DiseasesMale Urogenital Diseases

Criteria

Registry Platform Study Basic Inclusion \& Exclusion Criteria: Inclusion Criteria: 1. Aged ≥ 18 years at enrollment; 2. Patients who meet the diagnostic criteria for CKD; 3. Last eGFR ≥ 20 and \< 90 mL/min/1.73 m2 (with the CKD-EPI formula) within 12 months prior to enrollment; 4. Patients who voluntarily participate in this study and has signed and dated the informed consent form for the study; Exclusion Criteria: 1. Patients who have previously undergone/are undergoing/are planning to undergo solid organ transplantation; 2. Patients with active malignant tumor requiring drug therapy at the time of screening; 3. Women who are pregnant, planning to become pregnant or who are breastfeeding. Group A (Participants with CKD and High Proteinuria) Inclusion \& Exclusion Criteria: Inclusion criteria: Last documented proteinuria test within 12 months prior to enrollment indicating UACR ≥ 700 mg/g, or UPCR ≥ 1000 mg/g, or 24 h urine protein (quantitative) ≥ 1 g/24 h. Exclusion criteria: 1. Patients with NYHA class III or IV heart failure at screening; 2. Patients who have had myocardial infarction, unstable angina, stroke, transient ischemic attack (TIA), or undergone cardiac surgery, percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG), valvular repair/replacement, or received treatment with left ventricular assist device within 3 months prior to screening; 3. Patients undergoing renal replacement therapy (RRT) at screening; 4. Patients on systemic immunosuppression at screening (inhalation, intranasal administration, or topical steroids are allowed) except for stable maintenance therapy. The stable maintenance therapy means treatment at least 3 months with Prednisone 10mg/day or lower (or equivalent dose of other drugs), Azathioprine 100mg/day or lower, or Mycophenolate mofetil 1000mg/day or lower (or equivalent dose of other drugs); 5. Patients with a life expectancy of less than 1 year, as judged by the investigator; 6. Patients who have participated in another interventional clinical trial and have received the investigational drug within 1 month prior to being enrolled. Group B (patients with CKD and Hypertension) Inclusion \& Exclusion Criteria: Inclusion criteria: 1. Last documented test within 12 months prior to enrollment indicating UACR\>200 mg/g(22.6 mg/mmol)and \<5000 mg/g(565 mg/mmol), or UPCR \>500 mg/g and \<8000 mg/g, or 24 h urine protein (quantitative) \>0.5 g/24 h and \<8 g/24 h; 2. Patients with hypertension history and Systolic Blood Pressure ≥130 mmHg at screening; Exclusion criteria: 1. Patients with NYHA class IV heart failure at screening; 2. Patients who have had stroke, transient ischemic attack (TIA), Carotid artery surgery or carotid angioplasty and stenting, acute Coronary Syndrome, or hospitalization caused by heart failure deterioration within 3 months prior to screening; 3. Patients who have known severe hepatic injury (defined as Child-Pugh class C) based on medical history; 4. Patients undergoing renal replacement therapy (RRT) within 12 weeks prior to screening; 5. Patients on systemic immunosuppression prior to screening (inhalation, intranasal administration, or topical steroids are allowed) except for stable maintenance therapy at least 3 months; 6. Patients with a life expectancy of less than 1 year, as judged by the investigator; 7. Patients who have participated in another interventional clinical trial and have received the investigational drug within 1 months prior to being enrolled.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 41 locations

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Research Site

Baotou, ChinaOpen Research Site in Google Maps
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Research Site

Beijing, China
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Research Site

Changsha, China
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Research Site

Changzhou, China
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41 Study Centers