Improving heart failure treatment with advanced imaging techniques
Official title: Optimization of Cardiac Resynchronization Therapy by Non-Invasive Imaging of Cardiac Electrophysiology: A Pilot Study
Run by Medical University Innsbruck · NCT04662970 · Data updated 2026-11-12
This study is testing if using advanced imaging techniques can improve heart failure treatment by helping doctors better program heart devices for patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 25 (estimated) |
| Sponsor | Medical University Innsbruck Academic / other |
| Locations | 1 site (Innsbruck, Tyrol) |
| Status | Recruiting |
| Started | January 1, 2020 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | October 2, 2025 |
| Trial ID | NCT04662970 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients who have successfully received a CRT-D or CRT-P device and can undergo cardiac magnetic resonance imaging.
✕Probably not a fit
Patients with high-grade AV block, terminal heart failure, or contraindications to cardiac magnetic resonance imaging may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to enhance cardiac resynchronization therapy (CRT) by analyzing the activation times of the left and right ventricles using non-invasive imaging techniques. It utilizes patient-specific anatomical data obtained from cardiac magnetic resonance imaging to create a semi-automated model that incorporates the conductivity of various tissues. The study employs a software package to calculate local activation times, which will help optimize CRT device programming algorithms for better patient outcomes.
Why it matters
Potential benefit: If successful, this approach could lead to more effective heart failure treatments through personalized CRT programming.
How similar studies have gone: While this approach is innovative, similar studies have shown promise in optimizing cardiac therapies through advanced imaging techniques.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients after successful implantation of a CRT-D or CRT-P device in whom a cardiac magnetic resonance examination is possible and the device is equipped with the SyncAV® programming software * left bundle branch block before CRT implantation * PQ interval ≤ 250 ms before implantation Exclusion Criteria: * high-grade AV block * any contraindication concerning a safe CMR performance including claustrophobia * terminal heart failure (NYHA IV) or cardiac decompensation * life expectancy \< 1 year * women with child-bearing potential, pregnancy * drug abusus
Where it's running
-
Medical University Innsbruck
Innsbruck, Tyrol, Austria Recruiting
Study contacts
- Principal investigator: Wolfgang Dichtl, MD PhD — Medical University Innsbruck
- Study coordinator: Wolfgang Dichtl, MD PhD
- Email: dichtl@me.com
- Phone: 004351250481388
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.