INdobufen Versus asPirin in Endovascular Unruptured Intracranial Aneurysms Treatment (INPUT)

Inclusion criteria

• Age 18-75 years (male or female);
• Radiologically confirmed saccular intracranial aneurysm (by specialist assessment);
• Scheduled for endovascular embolization (including: coil embolization with stent assistance or flow diversion);
• Signed informed consent obtained.

Exclusion criteria

• Concomitant vascular malformations, tumors, abscesses or other cerebral diseases such as multiple sclerosis;
• Major surgery within 30 days prior to enrollment including fracture surgery or hip replacement;
• History of ischemic stroke, ischemic heart disease or hemorrhagic disorders including intracranial hemorrhage, gastrointestinal bleeding, fundus hemorrhage or unexplained bleeding within the past 6 months;
• Planned elective surgery within 3 months after the procedure;
• Any hematologic disorders or inherited coagulation abnormalities;
• Severe renal or hepatic dysfunction;
• History of hemostatic disorders, systemic bleeding, thrombocytopenia or neutropenia;
• History of symptomatic non-traumatic intracranial hemorrhage or cerebral amyloid angiopathy;
• Severe cardiopulmonary diseases considered by investigators to be unsuitable for the study;
• Women of childbearing potential with negative pregnancy test but refusing contraceptive measures, or those who are pregnant or lactating;
• Current participation in other investigational drug or device trials.

Withdrawal Criteria:

• Receiving aneurysm treatment other than coil embolization with stent assistance or flow diversion;
• Occurrence of endpoint events during stent-assisted aneurysm embolization procedure (as adjudicated by the Clinical Events Committee), including procedure-related hemorrhagic events (aneurysm rupture, parent artery rupture, subarachnoid hemorrhage, acute ipsilateral intracerebral hemorrhage, and acute ipsilateral subdural/epidural hematoma) or ischemic events (acute large vessel occlusion, in-stent thrombosis, and diffuse ipsilateral vascular infarction caused by plaque dislodgement);
• Device-related quality issues during stent-assisted embolization, including stent problems (stent fracture, failure to deploy properly, incomplete expansion due to product defect) and coil problems (premature detachment before intentional deployment, coil unraveling, and failure to detach);
• Postoperative life expectancy <3 months;
• Inability to complete 5-day premedication due to emergency surgery or other reasons;
• Intolerance to oral antiplatelet therapy due to allergy or other contraindications.