Integrated Diagnosis and Treatment of CKD on Outcomes

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorCapital Medical University

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 volunteers

Qualifiers

≥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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Integrated diagnosis and treatment for CKD

    Other intervention

    This 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

1,000 Participants
are divided into 2 treatment groups
Group A: Integrated group1 intervention
Group B: Unintegrated group1 intervention

Trial outcomes

Primary outcomes

1

Rate of cardiovascular cerebrovascular adverse events

Acute myocardial infarction, heart failure, shock, cardiac arrest, stroke, and lower limb arterial occlusion occurred during follow-up

Time frame
Six months or more

Secondary outcomes

1

Rate of all-cause mortality

Deaths from all causes during follow-up

Time frame
Six months or more

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Capital Medical University

Lead sponsor

Peking University

Sponsor institution