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Study identifier: NCT05564793 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Improving CRT Outcome With Non-Invasive Cardiac Mapping

Condition: Heart Failure With Reduced Ejection Fraction  ·  Sponsor: EP Solutions SA

PhaseNA
Planned participants330
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

The ICONIC-M study is a multicenter randomized controlled study to assess patient response to CRT comparing ECGI map guided left ventricular lead placement with empirical lead placement. The hypothesis of the investigation is to demonstrate that CRT LV lead implantation guided by a map obtained with the Amycard 01C System and showing LV Latest Electrical Activated Site (LEAS) in combination with a CT cardiac venogram improves CRT outcome. An improved CRT outcome is defined as a ≥30% increase in LVESVi reduction compared to empiric CRT LV lead implantation. The sample size will be 136 in the Control arm and 194 in the Active arm. A total of 330 subjects. The study follows an adaptive design, in where one interim analysis at 70% enrollment will be performed. The sponsor may stop enrollment when either one of the following conditions apply: * Statistical significant difference between groups in the primary endpoint has been reached confirming a difference in reduction of the LVESVi of ≥30% in the Active arm compared to the Control arm * There is no trend or reason to believe statistical significance will be reached with a higher sample size. Statistical significance (primary endpoint) is reached at interim (70%) or at total (100%) of enrollment with a significance value P lower than 0.025.

This description comes directly from the study's public registry record.

Talk to the study team

Matthias Egger, PhD  ·  +41 78 659 22 75  ·  matthias.egger@ep-solutions.ch

Adrian Maciejewski, Dr  ·  adrian.maciejewski@ep-solutions.ch

Always discuss trial participation with your own doctor first.

Locations (11)

Amsterdam University Medical CenterAmsterdam, NetherlandsNot Yet Recruiting
Groningen University Medical CenterGroningen, NetherlandsNot Yet Recruiting
Leids Universitair Medical CenterLeiden, NetherlandsNot Yet Recruiting
Maastricht University HospitalMaastricht, NetherlandsRecruiting
Utrecht University Medical CenterUtrecht, NetherlandsNot Yet Recruiting
Hospital da LuzLisbon, PortugalNot Yet Recruiting
Lund University HospitalLund, SwedenNot Yet Recruiting
Karolinska University HospitalStockholm, SwedenNot Yet Recruiting
Bart's HospitalLondon, United KingdomNot Yet Recruiting
King's CollegeLondon, United KingdomNot Yet Recruiting
Oxford University HospitalOxford, United KingdomNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT05564793