- Severe Complications During Ventricular Tachycardia or Premature Ventricular Complex Ablation — Recruiting • Cardiology / Cardiovascular • NCT07777744.
- What is being tested: This observational study characterizes severe complications occurring during ventricular tachycardia (VT) and premature ventricular complex (PVC) ablation procedures, collecting retrospective patient-level data on complication features, procedural factors, and clinical management strategies.
- Patient eligibility overview: The study includes patients who have experienced severe complications during VT/PVC ablation procedures; specific inclusion criteria relate to complication severity and procedure type rather than baseline patient demographics.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
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.
- : * Centers : Centers participating in the present collaborative study group. Invitation to participate will be based either upon personal referral of one of the investigator, previous collaboration or based on a meta-analytic review of the literature published on the subject within the past 20 years. * Patients: Females and males of >18 years undergoing any type of VT/PVC ablation. While we will accept redo-procedure we will ask for a unique patient-identifier to link procedures belonging to the same patients together. * Interventions: VT/PVC ablation (first intervention or re-do) as routinely performed by the participating centers * Outcomes: Severe complications, defined as hemodynamic instability requiring mechanical intensive-care management, tamponade, stroke, cardiac arrest, myocardial infarction, phrenic nerve palsies, major bleeding requiring transfusion, vascular or cardiac complication requiring surgery, procedure-related death. * Setting: Observational cohort studies, registries, retrospective cohort studies. Data stemming from RCTs (Randomized controlled trials) will not be collected as they likely do not represent a "real-life" setting. * Length of follow-up: Peri-procedural complications * Years considered: Not limited to a specific time-frame, but to reflect common ablation practices, we will focus on data from the 20 past years. * Number of patients provided : No lower limit…
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.