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Набор скоро начнётся NCT07522424

Comparison and Analysis of Functionality, Safety, Cost-effectiveness, and Environmental Impact of Reprocessed and New Ablation Catheters in Electrophysiological Procedures.

Без фазы С лечением Arhythmia

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Ablation - new, Ablation - reprocessed.
Кому может быть актуально
Состояния в реестре: Arhythmia. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Хорватия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

This study evaluates whether re-sterilized (reprocessed) ablation catheters are as effective and safe as new ablation catheters when used for electrophysiological procedures. Adult patients scheduled for catheter ablation will be randomly assigned to undergo the procedure using either a new catheter or a re-sterilized catheter, with identical procedural techniques applied in both groups. The study will compare procedural efficiency, safety, costs, and environmental impact between the two approaches. The results may support more sustainable and cost-effective use of medical devices in cardiac electrophysiology.

Подробное описание

This is a prospective, randomized, controlled non-inferiority trial comparing re-sterilized (reprocessed) and new ablation catheters in electrophysiological procedures. The study will be conducted at University Hospital Dubrava, a high-volume tertiary center for cardiac electrophysiology.

Patients scheduled for electrophysiological procedures will be randomized in a 1:1 ratio using a computer-generated sequence to undergo ablation with either a new or a re-sterilized catheter. All procedures will be performed by experienced electrophysiologists in accordance with standard institutional practice.

Procedure duration will be measured from groin puncture to completion of ablation. Additional procedural parameters related to ablation delivery, including duration and number of energy applications, total ablation time, and other procedural timing characteristics, will also be recorded. Fluoroscopy time and radiation dose, expressed as dose-area product (DAP), will be recorded automatically.

Catheter performance will be assessed based on achievement ablation, the number of energy applications and procedural assessment of catheter integrity, flexibility, and electrical properties.

Procedural safety will be evaluated by monitoring peri-procedural and post-procedural adverse events, including pericardial effusion, stroke, vascular complications, and death. Laboratory markers of inflammation, infection, and hemolysis will be obtained at predefined time points before and after the procedure. Blood cultures will be collected before and after the procedure to assess potential infectious complications.

Patients will be followed clinically during hospitalization and after discharge through telephone contact and routine outpatient visits.

Economic evaluation will include direct procedural costs, catheter costs, and re-sterilization costs. Environmental impact will be assessed based on medical waste generation and estimated carbon footprint associated with catheter use.

Re-sterilization of ablation catheters will be performed according to the validated internal protocol of University Hospital Dubrava, which has been used in routine clinical practice.

Вмешательства

  • Процедура Ablation - new
    Participants will undergo electrophysiological procedure (ablation). The intervention consists of the use a new ablation catheter. The key distinguishing feature of this intervention is the comparison of reprocessed versus new single-use catheters, while all other procedural aspects, including operator technique, energy delivery protocol, and peri-procedural care, are standardized and identical between groups.
  • Процедура Ablation - reprocessed
    Participants will undergo electrophysiological procedure (ablation). The intervention consists of the use of a reprocessed ablation catheter. The reprocessed catheter has undergone validated cleaning, resterilization, and functional testing in accordance with regulatory and safety standards prior to reuse. The key distinguishing feature of this intervention is the comparison of reprocessed versus new single-use catheters, while all other procedural aspects, including operator technique, energy d

Первичные конечные точки

  • Ablation duration [Срок оценки: From the start of the index ablation procedure until its completion.]
Вторичные конечные точки (7)
  • Acute Procedural Success [Срок оценки: From the start of the index ablation procedure until its completion]
  • Medical Waste Generated Per Procedure [Срок оценки: Periprocedural]
  • Fluoroscopy Time [Срок оценки: From the start of the index ablation procedure until its completion]
  • Radiation Dose (Dose-Area Product) [Срок оценки: From the start of the index ablation procedure until its completion]
  • Incidence of Peri- and Post-Procedural Complications [Срок оценки: Up to 30 days following the index ablation procedure]
  • Direct Procedural Costs Per Patient [Срок оценки: Periprocedural]
  • Estimated Carbon Footprint Per Procedure [Срок оценки: From the start of the index ablation procedure until its completion.]

Критерии участия

Критерии включения

  • Age ≥ 18 years
  • Indication for ablation according to current clinical guidelines
  • Written informed consent

Критерии исключения

  • Severe valvular heart disease
  • Significant structural heart disease that precludes (or makes ablation not feasible)
  • Pregnancy or breastfeeding
  • Life expectancy < 12 months

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Хорватия · 1 центр
  • UH Dubrava — Zagreb

Идентификаторы

NCT: NCT07522424 · 2026/0306

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗