Actively Recruiting

Age: 18Years - 100Years
All Genders
ID05242055

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

Led by Capital Medical University · Updated on 2022-05-06

1000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting an observational study to follow a group of patients with Chronic Kidney Disease (CKD) to evaluate how well integrated diagnosis and treatment based on guidelines is being applied in real-world clinical practice. The study aims to understand the clinical outcomes of patients with different risk levels by analyzing long-term follow-up data. This research focuses on CKD patients who may also have conditions like hypertension, hyperglycemia, hyperlipidemia, anemia, mineral and bone disorders, and malnutrition. The study divides participants into two groups: those receiving integrated diagnosis and treatment according to established guidelines, which includes regular monitoring and management of blood pressure, blood glucose, lipids, anemia, bone metabolism, nutrition, acid-base balance, electrolytes, diet, and exercise; and those receiving less comprehensive or unintegrated care. The integrated care group follows recommendations from Kidney Disease Improving Global Outcomes and the Chinese Medical Association guidelines during their follow-up period. Participants will be followed over time with ongoing clinical monitoring to assess outcomes such as the rate of cardiovascular and cerebrovascular adverse events, as well as all-cause mortality, measured over six months or longer. The research involves collecting data on how well integrated care is implemented in practice and analyzing risk factors to help improve CKD diagnosis, treatment quality, and patient prognosis. The observation will provide valuable data to support continuous improvement in CKD management in real-world settings.

CONDITIONS

Brief Title

Integrated Diagnosis and Treatment of CKD on Outcomes

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years old or older
  • Voluntarily signed informed consent
  • Patients who are estimated to develop CKD
Not Eligible

You will not qualify if you...

  • Age under 18 or over 100 years
  • Unable to comply with the procedures stipulated in this study
  • Estimated follow-up time less than 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Six months or more

Participants who undergo routine care are observed with integrated diagnosis and treatment or usual care during follow-up to monitor clinical outcomes.

Regular follow-up visits according to clinical practice

Trial Site Locations

Total: 1 location

1

Nephrology Department of Beijing Jishuitan Hospital

Beijing, Beijing Municipality, China, 100035

Actively Recruiting

Loading map...

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Similar Trials

"Smart Family Doctor" Assisted Comprehensive Management of S...

Post Coronary Artery Bypass Grafting

Actively Recruiting

1 location

The PILI 'Aina Project to Improve Cardiometabolic Health in...

Type 2 Diabetes

Actively Recruiting

2 locations

129Xe Gas Exchange MRI to Visualize Cardiopulmonary Function

Interstitial Lung Disease

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here