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Recruiting NCT06542016

NCT06542016 An Evaluation of the KCCQ Score in Predicting Cardiovascular Risk in Dialysis Patients

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Clinical Trial Summary
NCT ID NCT06542016
Status Recruiting
Phase
Sponsor Shenzhen Second People's Hospital
Condition Chronic Kidney Disease Stage 5
Study Type OBSERVATIONAL
Enrollment 136 participants
Start Date 2024-07-01
Primary Completion 2026-05-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 136 participants in total. It began in 2024-07-01 with a primary completion date of 2026-05-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Cardiovascular Disease (CVD) is the main complication and the most important cause of death in CKD patients. As the disease progresses, the incidence of cardiovascular disease in CKD patients gradually increases, especially in End-Stage Renal Disease (ESRD) patients receiving dialysis treatment, where the prevalence of cardiovascular disease reaches its highest level. Currently, there is a lack of a simple and reliable tool to assess the cardiac function status and predict the risk of cardiovascular events in patients on maintenance dialysis. The Kansas City Cardiomyopathy Questionnaire (KCCQ) is a widely used patient-reported outcomes measurement tool for assessing health-related quality of life in heart failure patients. It has been shown that KCCQ scores not only reflect the underlying undiagnosed symptoms of heart failure in CKD patients, but also have a strong correlation with prognosis. However, there is currently insufficient clinical evidence to confirm the value of the KCCQ in patients on maintenance dialysis. Investigators will perform a prospective, single-center, observational study to collect the changing trend of KCCQ scores at baseline and during the observation periods in maintenance dialysis patients, to analyze the association between the scores and the occurrence of long-term cardiovascular events and all-cause mortality. The aim is to construct a predictive model of KCCQ scores to provide a reference basis for clinical management of this high-risk group, so as to optimize the diagnosis and treatment of heart failure in dialysis patients and improve their cardiovascular outcomes.

Eligibility Criteria

Inclusion Criteria: 1. Age 18 or older with no restrictions on gender or ethnicity; 2. All enrolled patients meet the diagnostic criteria for CKD stage 5 according to the KDOQI guidelines of the National Kidney Foundation; 3. Newly diagnosed uremia patients planning to start maintenance dialysis (hemodialysis or peritoneal dialysis), as well as patients currently undergoing maintenance dialysis treatment (hemodialysis or peritoneal dialysis); 4. Clear contact information is available to reach patients or family members for follow-up; 5. Signed informed consent and ability to complete the KCCQ. Exclusion Criteria: 1. Patients with acute kidney injury from various causes; 2. Patients with severe mental illnesses that affect their ability to complete questionnaires; 3. Patients who have had acute myocardial infarction, coronary artery stent implantation, coronary artery bypass grafting (CABG) or pacemaker implantation within the past three months; 4. Patients with special types of heart disease, including cardiac amyloidosis, congenital heart disease and pericardial diseases; 5. Patients with chronic lung diseases; 6. Patients with serious underlying conditions such as severe infections, tumors or severe liver diseases; 7. Patients scheduled for kidney transplantation.

Contact & Investigator

Central Contact

Yi Xu

✉ xuyi20001234@163.com

📞 +8613798309505

Principal Investigator

QiJun Wan

STUDY DIRECTOR

Shenzhen Second People's Hospital

Frequently Asked Questions

Who can join the NCT06542016 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Chronic Kidney Disease Stage 5. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06542016 currently recruiting?

Yes, NCT06542016 is actively recruiting participants. Contact the research team at xuyi20001234@163.com for enrollment information.

Where is the NCT06542016 trial being conducted?

This trial is being conducted at Guangdong, China.

Who is sponsoring the NCT06542016 clinical trial?

NCT06542016 is sponsored by Shenzhen Second People's Hospital. The principal investigator is QiJun Wan at Shenzhen Second People's Hospital. The trial plans to enroll 136 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology