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Estimation of the Prevalence of Microcirculatory Dysfunction in Uremic Cardiopathy Among Dialysis Patients

Estimation of the Prevalence of Microcirculatory Dysfunction in Uremic Cardiopathy Among Dialysis Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07608679
Acronym
PRE-COCO
Enrollment
30
Registered
2026-05-27
Start date
2027-09-01
Completion date
2028-09-01
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodyalysis

Keywords

microcirculatory disorders, hemodyalysis

Brief summary

Patients with end-stage renal disease have a high burden of cardiovascular mortality, yet ischemic heart disease is often asymptomatic and difficult to diagnose in this population. Recent data suggest that microvascular coronary dysfunction may contribute significantly to myocardial ischemia in dialysis patients, but its true prevalence remains unknown. This study aims to evaluate microcirculatory coronary impairment in hemodialysis patients using invasive coronary angiography with measurement of coronary flow reserve (CFR), index of microcirculatory resistance (IMR). The study will also describe the clinical and biological characteristics associated with microvascular dysfunction in this population, in order to better understand the mechanisms of uremic cardiomyopathy and improve cardiovascular risk stratification.

Interventions

DIAGNOSTIC_TESTTransthoracic ultrasound at rest

Transthoracic ultrasound at rest

DIAGNOSTIC_TESTCardiological stress test

Left to the discretion of the centre: dobutamine echocardiography or myocardial scintigraphy.

DIAGNOSTIC_TESTCoronary angiography

Even even if the stress test comes back normal (these tests appear to be less effective at diagnosing microcirculatory abnormalities)

Sponsors

Centre Hospitalier Departemental Vendee
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Patients who have been on haemodialysis for at least 6 months * Elevated troponin levels \> 40 ng/L in a sample taken whilst the patient was in a stable condition, dated within the last 3 months * Patients capable of understanding the protocol and who have given their written informed consent to participate in the research * Patients registered with the National Health Service or eligible for it

Exclusion criteria

* Age \> 90 years * Patient undergoing daily home haemodialysis * Symptomatic stage 3 or 4 peripheral arterial disease * Severe hypertrophic cardiomyopathy (genetic or amyloid) * Severe valvular heart disease leading to left ventricular remodelling (surgically contraindicated severe aortic stenosis, severe mitral regurgitation, severe aortic regurgitation) * Hospitalisation for decompensation/acute heart failure within the last month * Acute coronary syndrome and any coronary artery disease requiring angioplasty and/or stent implantation within the last 3 months * Contraindication to METHERGIN and DOBUTAMINE * Patients participating in another clinical research protocol that may affect the research objectives * Patients already included in the study * Patients under guardianship, curatorship or deprived of their liberty * Patients under an activated future protection order * Patients under family authorisation * Patient under judicial protection * Pregnant patient

Design outcomes

Primary

MeasureTime frame
Percentage of patients with microcirculatory heart disease (i.e. microvascular dysfunction or microvascular vasospasm) identified during coronary angiographyCardiac examinations to be carried out within 8 to 10 weeks of enrolment

Countries

France

Contacts

CONTACTChloé MOREAU
promotion.urc@chd-vendee.fr251446327
PRINCIPAL_INVESTIGATORGrégoire COUVRAT-DESVERGNES

Centre Hospitalier Departemental Vendee

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026