Stapf Christian
Department of Neurology, Hôpital Lariboisière (APHP), 2, Rue Ambroise Paré, Paris cedex 10, Paris, 75475, France.
Acta Neurochir Suppl. 2010;107:83-5. doi: 10.1007/978-3-211-99373-6_13.
A Randomized Trial of Unruptured Brain AVMs is a multidisciplinary international randomized controlled clinical trial including 800 adult patients with the diagnosis of an unruptured brain AVM. Patients willing to participate are randomly assigned to either best possible invasive therapy (endovascular, neurosurgical, and/or radiation therapy) or medical management without intervention. The study protocol does not modify any routine treatment strategies in either arm. Patients will be followed for a minimum of 5 years and a maximum of 10 years from randomization.The primary outcome measure is the composite endpoint of death from any cause or stroke (clinically symptomatic hemorrhage or infarction confirmed by imaging). The secondary outcome measure is long-term clinical status by Rankin Scale, NIHSS, SF-36, and EuroQol.Patient enrollment was successfully started in 2007. Participating sites currently include multidisciplinary treatment centers in North and South America, Australasia, and Europe (including Australia, Austria, Brazil, Canada, Finland, France, Germany, Italy, Netherlands, Spain, South Korea, Switzerland, UK, and the USA).The trial is sponsored and monitored by the US NIH/NINDS (NCT00389181).
未破裂脑动静脉畸形随机试验是一项多学科国际随机对照临床试验,纳入800例诊断为未破裂脑动静脉畸形的成年患者。愿意参与的患者被随机分配至最佳侵入性治疗组(血管内治疗、神经外科手术和/或放射治疗)或非干预性药物治疗组。研究方案不改变任何一组的常规治疗策略。患者将从随机分组开始随访至少5年,最长10年。主要结局指标是任何原因导致的死亡或卒中(经影像学证实的临床症状性出血或梗死)的复合终点。次要结局指标是采用Rankin量表、美国国立卫生研究院卒中量表(NIHSS)、36项简明健康状况调查量表(SF-36)和欧洲五维度健康量表(EuroQol)评估的长期临床状态。患者入组于2007年成功启动。参与站点目前包括北美、南美、澳大拉西亚和欧洲的多学科治疗中心(包括澳大利亚、奥地利、巴西、加拿大、芬兰、法国、德国、意大利、荷兰、西班牙、韩国、瑞士、英国和美国)。该试验由美国国立卫生研究院/国立神经疾病与卒中研究所(NCT00389181)赞助和监督。