Transvenous Approach for the Treatment of cerebral Arteriovenous Malformations (TATAM): Study protocol of a randomised controlled trial

Author:

Fahed Robert1,Darsaut Tim E2,Mounayer Charbel3,Chapot René4,Piotin Michel1,Blanc Raphaël1,Mendes Pereira Vitor5,Abud Daniel G6,Iancu Dana7,Weill Alain7,Roy Daniel7,Nico Lorena7,Nolet Suzanne8,Gevry Guylaine8,Raymond Jean78ORCID

Affiliation:

1. Department of Interventional Neuroradiology, Fondation Rothschild Hospital, Paris, France

2. Department of Surgery, University of Alberta Hospital, Edmonton, Canada

3. Service de Neuroradiologie, CHU Dupuytren, Service de Neuroradiologie, Limoges, France

4. Department of Neuroradiology, Alfried-Krupp Krankenhaus Hospital, Essen, Germany

5. Department of Medical Imaging, Toronto Western Hospital, Toronto, Canada

6. Division of Interventional Neuroradiology, Medical School of Ribeirão Preto, University of São Paulo, Brazil

7. Department of Radiology, Centre Hospitalier de l’Université de Montréal (CHUM), Montreal, Canada

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.

Publisher

SAGE Publications

Subject

Immunology

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