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RecruitingNCT06143995CREATIVEUpdated Nov 22, 2023

The Diagnosis and Treatment Pattern of CKD in Patients With Cardiovascular Disease- a National Cross-sectional Study

An observational study in Renal Insufficiency, Chronic, Cardiovascular Diseases and Diagnosis, sponsored by Guangdong Provincial People's Hospital. Recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-11-22.

Sponsored by Guangdong Provincial People's Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2024, 2 years 3 months ago, but the record still lists the study as recruiting.
  • Started Jul 2023; still recruiting 3 years 3 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
2,000
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this observational study is to learn about in a total of approximately 2000 patients with cardiovascular disease recruited from about 25 participating sites in China with eGFR\<60 ml/min/1.73 m2 and/or UACR>30 mg/g at least twice 3 months apart within the previous 12 months who had been hospitalized in the cardiology department within the previous 12 months. The main questions it aims to answer are:

  • To estimate the diagnosis rate of CKD in patients with cardiovascular disease and laboratory evidence of CKD
  • To describe the CKD awareness and treatment pattern in patients with cardiovascular disease and laboratory evidence of CKD.
  • To describe the socio-demographic and clinical characteristics of CKD in patients with cardiovascular disease and laboratory evidence of CKD

Participants will be invited to undergo a baseline visit, and the demographics, lifestyle factors, clinical characteristics, and laboratory tests will be collected.

02

Conditions studied

  • Renal Insufficiency, Chronic
  • Cardiovascular Diseases
  • Diagnosis
03

In context

Renal Insufficiency

1,995 studies on the registry are indexed under Renal Insufficiency; 173 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 149 across 394 observational studies indexed under Renal Insufficiency.

Browse Renal Insufficiency studies →

Lead sponsor

Guangdong Provincial People's Hospital is the lead sponsor of 231 studies on the registry; 101 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

a total of approximately 2000 patients with cardiovascular disease recruited from about 25 participating sites in China

Inclusion criteria

  1. Female and/or male aged ≥18 years
  2. Admitted to the cardiology department with diagnosed cardiovascular disease within the previous 12 months
  3. Participants with eGFR\<60 ml/min/1.73 m2 and/or UACR>30 mg/g at least twice 3 months apart within the previous 12 months

Exclusion criteria

Exclusion Criteria:

  1. Participants with known eGFR\<20 ml/min/1.73 m2 or undergoing dialysis or kidney transplantation
  2. Pregnant or lactating women
  3. Exposure to contrast medium or other reason leading to potential acute kidney injury since the baseline examination of eGFR/UACR
  4. Patients who were participating in or had participated in any other clinical trial within the previous 12 months
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
2,000 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. CKD diagnosis rates

    CKD diagnosis rates in overall enrolled patients and subgroups (stratified by isolated estimated glomerular filtration rate (eGFR) measurement, isolated urinary albumin-to-creatinine ratio ( UACR) measurement, and both measurements) will be assessed in 12 month.

    Time frame: 1 day

Secondary outcomes

  1. Clinical characteristics

    Clinical characteristics in the overall participants and groups stratified by CKD diagnosis (CKD diagnosis, and CKD non-diagnosis) will be reported in 12 months.

    Time frame: 1 day

  2. CKD diagnosis/treatment rate

    CKD diagnosis/treatment rate in groups stratified by of disease types (HTN, Coronary artery disease (CAD), Heart Failure (HF), type 2 diabetes mellitus (T2DM), etc.) will be assessed in 12 months.

    Time frame: 1 day

  3. The number, types, treatment rates of medicine

    The number, types, treatment rates of medicine (by class) for renal protection or with potential renal contraindication, awareness in the overall enrolled participants and groups stratified by CKD diagnosis (CKD diagnosis, CKD non-diagnosis) will be reported in 12 months.

    Time frame: 1 day

07

Study locations

1 of 1 sites recruiting
  • Guangdong Provincial People's Hospital
    Guangzhou, Guangdong, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06143995
Lead sponsor
Guangdong Provincial People's Hospital
Responsible party
Sponsor
First posted
Nov 22, 2023
Start date
Jul 1, 2023
Primary completion
Jul 2024 (estimated)
Completion
Jul 2024 (estimated)
Last update
Nov 22, 2023

Study contacts

Chen Jiyan, PHD
Contact
Chen-jiyan@163.com
86-020-83827812-10528

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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