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Not yet recruitingNCT07585695EVACKDUpdated May 14, 2026

Coronary Artery Disease Screening in Patients With Chronic Kidney Disease

An observational study in Chronic Kidney Disease (CKD) and Coronary Artery Disease (CAD), sponsored by University Hospital, Grenoble. Not yet recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-14.

Sponsored by University Hospital, Grenoble · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
283
Ages
18 Years and older
Sex
All
01

Study summary

Patients with chronic kidney disease (CKD) have a markedly increased cardiovascular risk, with coronary artery disease being a leading cause of morbidity and mortality. Conventional cardiovascular risk scores and non-invasive diagnostic tests have limited accuracy in this population, partly due to atypical symptoms and frequent structural heart disease. Coronary flow reserve (CFR) is a key marker of coronary microvascular dysfunction and has strong prognostic value, but its assessment is usually limited to invasive techniques. Recent advances in cadmium-zinc-telluride single-photon emission computed tomography (CZT-SPECT) allow non-invasive measurement of CFR. The EVACKD study aims to evaluate the prognostic value of CFR assessed by CZT-SPECT in patients with CKD for predicting major adverse cardiovascular events over a 2-year follow-up.

02

Conditions studied

  • Chronic Kidney Disease (CKD)
  • Coronary Artery Disease (CAD)

Keywords

  • Chronic Kidney Disease
  • Coronary Flow Reserve
  • coronary artery disease
03

In context

Renal Insufficiency, Chronic

3,144 studies on the registry are indexed under Renal Insufficiency, Chronic; 704 are open to participants now.

This study's planned enrollment of 283 is above the median of 200 across 867 observational studies indexed under Renal Insufficiency, Chronic.

Browse Renal Insufficiency, Chronic studies →

Lead sponsor

University Hospital, Grenoble is the lead sponsor of 815 studies on the registry; 205 are open to participants now.

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

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Who can participate

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

Study population

Patients from the University Hospital of Grenoble

Inclusion criteria

  • Male or female patients aged over 18 years
  • Affiliated with the French social security system
  • Patients at renal risk based on albuminuria (Alb) and glomerular filtration rate (GFR \< 30 mL/min/1.73 m², or GFR \< 45 mL/min/1.73 m² with albuminuria > 30 mg/g, or GFR \< 60 mL/min/1.73 m² with albuminuria > 300 mg/g)
  • Patients undergoing, independently of the research and according to the clinician's decision as part of standard care, CZT-SPECT myocardial perfusion imaging with coronary flow reserve measurement for cardiovascular risk assessment
  • Having expressed no objection to participation in this study

Exclusion criteria

Exclusion Criteria:

  • Legally protected adult (Article L1121-8 of the French Public Health Code)
  • Person deprived of liberty (Article L1121-8 of the French Public Health Code)
  • Pregnant woman
  • Patient who has undergone a normal coronary exploration within the past year
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
283 participants (estimated)
Target follow-up
25 Months
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. To assess the prognostic value of impaired coronary flow reserve measured by CZT myocardial perfusion imaging

    Composite endpoint including cardiac mortality, non-fatal myocardial infarction, non-fatal ischemic stroke, and hospitalization for heart failure.

    Time frame: 2-year follow-up

Secondary outcomes

  1. To assess the prognostic value of coronary flow reserve to each individual component of the primary endpoint

    To evaluate each component separately : Cardiac mortality rate, non-fatal myocardial infarction rate, non-fatal ischemic stroke rate, hospitalization rate for heart failure, and all-cause mortality rate.

    Time frame: 2 years

  2. To assess the prognostic value of coronary flow reserve for Major Adverse Kidney Events (MAKE)

    Rate of patients with Major Adverse Kidney Events (MAKE), defined by the composite endpoint of death, dependence on renal replacement therapy, and a ≥50% decline in estimated glomerular filtration rate (eGFR) from baseline

    Time frame: At 1-year and 2-year follow-up

  3. To assess the number of Acute Kidney Injury (AKI) events during follow-up

    Evaluation of the Acute Kidney Injury (AKI) rate classified into three grades: Grade 1 (1.5- to 2-fold increase in serum creatinine), Grade 2 (2- to 3-fold increase), and Grade 3 (\>3-fold increase or need for dialysis)

    Time frame: 2 years

  4. To assess the number of coronary revascularizations by coronary artery bypass grafting or percutaneous coronary intervention

    Performed by calculating the rate of revascularization by coronary artery bypass grafting or percutaneous coronary intervention

    Time frame: 2 years

  5. To assess the prevalence of ischemic heart disease without significant coronary artery stenosis (INOCA)

    Rate of ischemic heart disease without significant coronary artery stenosis (INOCA)

    Time frame: 2 years

07

Study locations

1 site
  • CHU Grenoble Alpes
    La Tronche, France 38700, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07585695
Lead sponsor
University Hospital, Grenoble
Responsible party
Sponsor
First posted
May 14, 2026
Start date
Jun 1, 2026 (estimated)
Primary completion
Nov 30, 2027 (estimated)
Completion
Jan 31, 2028 (estimated)
Last update
May 14, 2026

Study contacts

Gilles Barone Rochette
Contact
gbarone@chu-grenoble.fr
+33476765172
Clémence Charlon
Contact
ccharlon@chu-grenoble.fr
+33476766652

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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