ACTRN12622001080718尚未招募未知
A Prospective Cohort Study assessing the feasibility, efficacy and safety of Cardiac Stereotactic Body Radiotherapy (SBRT) in patients with Ventricular Tachycardia (VT)
Metro South Hospital0 个研究点目标入组 10 人开始时间: 2022年8月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Documented sustained ventricular tachycardia (VT) with at least 3 episodes of VT in 12 months prior to enrollment
- •Require at least 1 anti-arrhythmic medication
- •Failed at least 1 invasive catheter ablation procedure, or have contraindications to invasive catheter ablation
- •Assessed as able to tolerate radiotherapy planning, immobilisation and treatment as deemed by the radiation oncologist
- •Willing and able to provide informed consent
排除标准
- •Previous radiotherapy to the chest with any radiation dose to the heart
- •Advanced heart failure (NYHA Class IV)
- •High-volume myocardial scar substrate to such an extent that treatment with Stereotactic Body Radiotherapy (SBRT) is deemed unsafe by the radiation oncologist
- •Ventricular Tachycardia (VT) deemed not to be related to a definable myocardial scar
- •Competing comorbidities (unrelated to VT) which limit life expectancy to less than 6 months.
- •Must not be pregnant and/or breastfeeding if female; must have a negative pregnancy test within 7 days of study enrollment.
- •Implantable Cardiac Defibrillator (ICD) implanted less than 6 weeks prior
- •Renal failure or allergy precluding administration of Intravenous (IV) gadolinium
- •Computer Tomography (CT) IV contrast allergy
- •Any concurrent anti-neoplastic therapy
研究者
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