Integrated Diagnosis and Treatment of CKD on Outcomes

  • STATUS
    Recruiting
  • End date
    Dec 31, 2026
  • participants needed
    1000
  • sponsor
    Capital Medical University
Updated on 9 May 2022
cardiovascular disease
anemia
malnutrition
renal disease
blood lipids

Summary

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.

Details
Condition Chronic Kidney Diseases, Hypertension, Hyperglycemia, Hyperlipidemias, Anemia, Chronic Kidney Disease-Mineral and Bone Disorder, Malnutrition
Treatment Integrated diagnosis and treatment for CKD
Clinical Study IdentifierNCT05242055
SponsorCapital Medical University
Last Modified on9 May 2022

Eligibility

Yes No Not Sure

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
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