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Recruiting NCT05242055

Integrated Diagnosis and Treatment of CKD on Outcomes

Observational Chronic Kidney Diseases Hypertension Hyperglycemia Hyperlipidemias

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Integrated diagnosis and treatment for CKD.
Who it may be relevant to
Registry conditions: Chronic Kidney Diseases, Hypertension, Hyperglycemia, Hyperlipidemias. Basic parameters: 18 years — 100 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Prospective, Cohort, and Observational Study of the Effect of Integrated Diagnosis and Treatment of Chronic Kidney Disease (CKD) on Clinical Outcomes in Real World Clinical Practice

Overview

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.

Interventions

  • Other Integrated diagnosis and treatment for CKD
    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.

Primary outcome measures

  • Rate of cardiovascular cerebrovascular adverse events [Time frame: Six months or more]
Secondary outcome measures (1)
  • Rate of all-cause mortality [Time frame: Six months or more]

Eligibility criteria

Inclusion criteria

  • ≥18 years old;
  • Voluntarily signed informed consent;
  • Patients who are estimated to develop CKD.

Exclusion criteria

  • Age < 18 or ≥100 years;
  • Unable to comply with the procedures stipulated in this study;
  • Estimated follow-up time ≤6 months.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Nephrology Department of Beijing Jishuitan Hospital — Beijing

Identifiers

NCT: NCT05242055 · 202112-11

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗