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Clinical Trials in Germany / NCT07018778
Starting soon Observational

CMR-derived Quantitative Perfusion for Prediction of FFR

NCT07018778 · tracked via the Priya Life Science Germany tracker
Sponsor
Kerckhoff Klinik
Phase
Observational
Started
2025-07-01
Last updated
2025-06-18

Condition(s) studied

Chronic Coronary Syndrome

Study summary

Patients will undergo quantitative perfusion assessment in cardiovascular magnetic resonance imaging (dual bolus or dual sequence approach) as well as invasive coronary angiography for assessment of fractional flow reserve (FFR) including assessment of coronary flow reserve (CFR) and microcirculatory resistance (IMR).

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria: * clinical indication for vasodilatator CMR or invasive coronar angiography * capability to give informed consent Exclusion Criteria: * general: non-compliance, \<18 years of age, pregnancy * contraindications for CMR (non-CMR compatible device, chronic kidney disease (eGFR \<30ml/min), allergies (medications)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kerckhoff Klinik Bad Nauheim Hesse

More Kerckhoff Klinik trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07018778 on ClinicalTrials.gov ↗ ← All trials in Germany