Robert Fahed1, Tim E Darsaut2, Charbel Mounayer3, René Chapot4, Michel Piotin1, Raphaël Blanc1, Vitor Mendes Pereira5, Daniel G Abud6, Dana Iancu7, Alain Weill7, Daniel Roy7, Lorena Nico7, Suzanne Nolet8, Guylaine Gevry8, Jean Raymond7,8. 1. 1 Department of Interventional Neuroradiology, Fondation Rothschild Hospital, Paris, France. 2. 2 Department of Surgery, University of Alberta Hospital, Edmonton, Canada. 3. 3 Service de Neuroradiologie, CHU Dupuytren, Service de Neuroradiologie, Limoges, France. 4. 4 Department of Neuroradiology, Alfried-Krupp Krankenhaus Hospital, Essen, Germany. 5. 5 Department of Medical Imaging, Toronto Western Hospital, Toronto, Canada. 6. 6 Division of Interventional Neuroradiology, Medical School of Ribeirão Preto, University of São Paulo, Brazil. 7. 7 Department of Radiology, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Canada. 8. 8 Interventional Neuroradiology Laboratory, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
Abstract
BACKGROUND:Transvenous embolisation is a promising technique but the benefits remain uncertain. We hypothesised that transvenous embolisation leads to a higher rate of arteriovenous malformation angiographic occlusion than transarterial embolisation. METHODS: The Transvenous Approach for the Treatment of cerebral Arteriovenous Malformations (TATAM) is an investigator initiated, multicentre, prospective, phase 2, randomised controlled clinical trial. To test the hypothesis that transvenous embolisation is superior to transarterial embolisation for arteriovenous malformation obliteration, 76 patients with arteriovenous malformations considered curable by up to two sessions of endovascular therapy will be randomly allocated 1:1 to treatment with either transvenous embolisation (with or without transarterial embolisation) (experimental arm) or transarterial embolisation alone (control arm). The primary endpoint of the trial is complete arteriovenous malformation occlusion, assessed by catheter cerebral angiography. Complete occlusions will be confirmed at 3 months, while incompletely occluded arteriovenous malformations, considered treatment failures, will then be eligible for complementary treatments by surgery, radiation therapy, or even transvenous embolisation. Standard procedural safety outcomes will also be assessed. Patient selection will be validated by a case selection committee, and participating centres with limited experience in transvenous embolisation will be proctored. DISCUSSION: The TATAM trial is a transparent research framework designed to offer a promising but still unvalidated treatment to selected arteriovenous malformation patients. Clinical Trial Registration-URL: http://www.clinicaltrials.gov . Unique identifier: NCT03691870.
RCT Entities:
BACKGROUND: Transvenous embolisation is a promising technique but the benefits remain uncertain. We hypothesised that transvenous embolisation leads to a higher rate of arteriovenous malformation angiographic occlusion than transarterial embolisation. METHODS: The Transvenous Approach for the Treatment of cerebral Arteriovenous Malformations (TATAM) is an investigator initiated, multicentre, prospective, phase 2, randomised controlled clinical trial. To test the hypothesis that transvenous embolisation is superior to transarterial embolisation for arteriovenous malformation obliteration, 76 patients with arteriovenous malformations considered curable by up to two sessions of endovascular therapy will be randomly allocated 1:1 to treatment with either transvenous embolisation (with or without transarterial embolisation) (experimental arm) or transarterial embolisation alone (control arm). The primary endpoint of the trial is complete arteriovenous malformation occlusion, assessed by catheter cerebral angiography. Complete occlusions will be confirmed at 3 months, while incompletely occluded arteriovenous malformations, considered treatment failures, will then be eligible for complementary treatments by surgery, radiation therapy, or even transvenous embolisation. Standard procedural safety outcomes will also be assessed. Patient selection will be validated by a case selection committee, and participating centres with limited experience in transvenous embolisation will be proctored. DISCUSSION: The TATAM trial is a transparent research framework designed to offer a promising but still unvalidated treatment to selected arteriovenous malformationpatients. Clinical Trial Registration-URL: http://www.clinicaltrials.gov . Unique identifier: NCT03691870.
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