TY - JOUR T1 - Statin treatment for unruptured intracranial aneurysms study: a study protocol for a double-blind, placebo-controlled trial JF - Stroke and Vascular Neurology JO - Stroke Vasc Neurol SP - 410 LP - 415 DO - 10.1136/svn-2020-000353 VL - 5 IS - 4 AU - Wenqiang Li AU - Yisen Zhang AU - Zhongbin Tian AU - Wei Zhu AU - Jian Liu AU - Ying Zhang AU - Xinjian Yang AU - De-Cai Tian Y1 - 2020/12/01 UR - http://svn.bmj.com/content/5/4/410.abstract N2 - Background and purpose A large proportion of patients with unruptured intracranial aneurysm (IA) are not suitable for surgical clipping and endovascular treatment. For these patients, anti-inflammatory medications are worth exploring due to inflammation of aneurysmal wall being a major factor in higher risk of rupture. Statin has been proven to reduce inflammation of atherosclerosis and maybe a suitable candidate. This study aimed to evaluate whether atorvastatin will reduce inflammatory of the aneurysm wall measured by the signal index of aneurysm wall enhancement.Methods and analysis The Statin Treatment for UnruptureD Intracranial anEurysms Study is a single-centre, phase 2, randomised, controlled, double-blind clinical trial. 60 patients with unruptured IAs with aneurysm wall enhancement will be enrolled in Beijing Tiantan Hospital. The patients will be randomised to receive atorvastatin 20 mg or placebo orally per day for 12 months. The primary outcome will be the change in aneurysm wall enhancement measured by the signal index during the 12 months treatment with atorvastatin. The secondary study outcomes will be the change in aneurysm wall enhancement measured by the signal index at 3 months, the changes in aneurysmal morphology and inflammation-related factors (C reactive protein, tumour necrosis factor-α, interleukin-1β and interleukin-6) at 3 and 12 months. This study is the first to explore the role of atorvastatin in reducing inflammation in unruptured IA, which could lay the groundwork for future phase III trial.Ethics and dissemination Beijing Tiantan Hospital’s Ethics committee approved the research and written informed consents would be obtained from all participant or representative included in this study.Trial registration number NCT04149483 ER -