Severe Complications During Ventricular Tachycardia or Premature Ventricular Complex Ablation (NCT07777744)
Severe Complications During Ventricular Tachycardia or Premature Ventricular Complex Ablation - an International Multicenter Collaborative Study Group
🩺 Plain-English Summary (8th-Grade Level)
The investigators aim to characterize patients presenting with a severe ventricular tachycardia (VT) and premature ventricular complex (PVC)-ablation-related complication including patient characteristics, procedural details and subsequent management of the complication by gathering existing patient-level data.
Who can join: Review the eligibility criteria below.
Location: Rush University Medical Center — Chicago, Illinois
Age range: 18 Years
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (25 Sites)
- Rush University Medical Center — Chicago, Illinois
- University of Michigan — Michigan Center, Michigan
- Medical University of Graz — Graz,
- Université Laval — Québec,
- The First Affiliated Hospital of Nanjing Medical University — Nanjing,
- University Hospital Center Sestre milosrdnice — Zagreb,
- CHU Bordeaux — Bordeaux,
- Centre Hospitalier Universitaire Trousseau — Chambray-lès-Tours,
- University Hospital Poitier — Poitiers,
- Clinique Pasteur Toulouse — Toulouse,
- Zentralklinik Bad Bercka — Bad Berka,
- Uniklinik Freiburg — Bad Krozingen,
- Carl-Thiem-Klinikum — Cottbus,
- Universitätsklinikum Münster — Münster,
- University of Patras — Pátrai,
- Sheba Medical Center — Ramat Gan,
- Citta della Salute e della Scienza di Torino — Torino,
- Mount Elisabeth Medical Centre — Singapore,
- University Medical Center Ljubljana — Ljubljana,
- Hospital Universitario Ramón y Cajal — Madrid,
- University Hospital Basel — Basel,
- Inselspital Bern — Bern,
- Ankara City Hospital — Ankara,
- Hacettepe University — Ankara,
- Royal Papworth Hospital — Cambridge,
📞 Contact the Study Coordinator
Phone: 0041 61 265 52 14
Email: Michael.kuehne@usb.ch
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.