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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.

Authors :
Hirai, Sakyo
Fujita, Kyohei
Fujii, Shoko
Takahashi, Satoru
Shigeta, Keigo
Karakama, Jun
Enomoto, Yukiko
Sato, Yohei
Yoshimura, Masataka
Hirota, Shin
Mizoue, Tatsuya
Yoshino, Yoshikazu
Kawano, Yoshihisa
Yamamura, Toshihiro
Kohyama, Shinya
Hirohata, Masaru
Yoshimura, Shinichi
Ishii, Yosuke
Yamauchi, Toshihiro
Taira, Naoki
Source :
PLoS ONE. 9/26/2024, Vol. 19 Issue 9, p1-11. 11p.
Publication Year :
2024

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
19
Issue :
9
Database :
Academic Search Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
179947682
Full Text :
https://doi.org/10.1371/journal.pone.0310906