About this trial
Objective: To establish a study cohort and follow up of patients with CKD in our hospital, and evaluate the status of integrated CKD diagnosis and treatment according to guidelines in the real world, as well as the clinical prognosis of patients with different stratification.
Methods: By establishing a cohort of 1000 patients with CKD and conducting long-term follow-up, integrated diagnosis and treatment for CKD was performed, namely: Regular monitoring, control of blood pressure, blood glucose, blood lipid, correction of anemia, minerals - bone metabolic abnormalities, malnutrition, acid and alkali, and electrolyte disorder, diet and exercise, such as the guidance of integrated management, non intrusive, observational studies, prospective cohort were analyzed retrospectively, describe the implementation of the integration of diagnosis and treatment, chronic kidney disease (CKD) Stratified analysis and risk factor analysis were performed for cardiovascular disease and other main endpoint events, so as to objectively reflect the status of integrated treatment of CKD and provide data support for continuous quality improvement of CKD diagnosis and treatment and improvement of clinical prognosis of patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
≥18 years old;
Voluntarily signed informed consent;
Patients who are estimated to develop CKD.
Disqualifiers
Age < 18 or ≥100 years;
Unable to comply with the procedures stipulated in this study;
Estimated follow-up time ≤6 months.
Trial population
Patients with CKD following up more than 6 months in Beijing Jishuitan Hospital.
Trial design
Cohort
Prospective
Treatments tested in this trial
Integrated diagnosis and treatment for CKD
Other interventionThis is an observational study. Investor will not intervene the clinical practice of doctors. In the real world, there would be many factors affect the proceeding of the guidelines contents. There will be integrated diagnosis and treatment during follow-up.
Treatment groups
Trial outcomes
Primary outcomes
Rate of cardiovascular cerebrovascular adverse events
Acute myocardial infarction, heart failure, shock, cardiac arrest, stroke, and lower limb arterial occlusion occurred during follow-up
Secondary outcomes
Rate of all-cause mortality
Deaths from all causes during follow-up
Sponsors and contacts
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Capital Medical University
Lead sponsor
Peking University
Sponsor institution