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Study protocol of the ASTOP trial: A multicenter, randomized, double-blind, placebo-controlled trial of presurgical aspirin administration for the prevention of thromboembolic complications of coil embolization for ruptured aneurysms

2024; Public Library of Science; Volume: 19; Issue: 9 Linguagem: Inglês

10.1371/journal.pone.0310906

1932-6203

Sakyo Hirai, Kyohei Fujita, Shoko Fujii, Satoru Takahashi, Keigo Shigeta, Jun Karakama, Yukiko Enomoto, Yohei Sato, Masataka YOSHIMURA, Shin Hirota, Tatsuya Mizoue, Yoshikazu Yoshino, Yoshihisa Kawano, Toshihiro Yamamura, Shinya Kohyama, Masaru Hirohata, Shinichi Yoshimura, Yosuke Ishii, Toshihiro Yamauchi, Naoki Taira, Yoshiki Obata, Makoto Sakamoto, Masato Inoue, Motoshige Yamashina, So Tokunaga, Toshio Higashi, Kana Sawada, Hidetoshi Mochida, Keisuke Ido, Masataka Takeuchi, Tomoji Takigawa, Yasushi Takagi, Masafumi Morimoto, Masataka Nanto, Kazunori Miki, Kouichi Misaki, Koichi Arimura, Yoshiki Hanaoka, Mutsuya Hara, Shoko Hara, Kota Yokoyama, Jun Ooyama, Ryoichi Hanazawa, Hiroyuki Sato, Akihiro Hirakawa, Megumi Ishiguro, Shigeru Nemoto, Kazutaka Sumita,

Acute Ischemic Stroke Management

Rationale Thromboembolism is a serious complication of endovascular treatment for ruptured cerebral aneurysms. The administration of antiplatelet agents before endovascular treatment for ruptured cerebral aneurysms may reduce the risk of thromboembolic complications. Aim This study aimed to assess the safety and efficacy of preoperative aspirin administration in endovascular treatment for ruptured cerebral aneurysms. Sample size estimates Assuming a 15% incidence rate of both intraoperative thromboembolic morbidity and symptomatic ischemic lesions on magnetic resonance imaging diffusion-weighted imaging scans assessed by an Independent Review Committee, a sample size of 484 will be required to detect a 10% improvement with aspirin administration with 90% power using the Pearson’s chi-square test at a two-sided significance level of 2.5% for each primary outcome, after accounting for a 5% dropout rate. Methods and design ASTOP is a multicenter, randomized, double-blind, placebo-controlled clinical trial. A total of 484 patients with ruptured cerebral aneurysms receiving coil embolization within 72 h of onset will be randomly assigned 1:1 to receive 200 mg of aspirin or placebo before the procedure. Study outcomes The primary outcomes will be the incidence rates of intraoperative thromboembolic complications and symptomatic ischemic lesions on magnetic resonance imaging diffusion-weighted imaging scans evaluated by the Independent Review Committee. The secondary outcomes will be the incidence rate of cerebral ischemic events and all bleeding events within 14 days of enrollment and functional outcomes defined by the modified Rankin Scale score at 90 days. Discussion This trial will provide valuable data on the role of antiplatelet agents during endovascular treatment for ruptured cerebral aneurysms. Trial registration Registration : Japan Registry of Clinical Trials, Identifier: jRCTs031210421 .