The study is a prospective, multi-center, single arm, feasibility study that will enroll a maximum of 20 subjects. A maximum of 5 investigational centers in Australia will participate. Enrollment is expected to take about 4 months, subject participation will last about 3 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
DAISe Thrombectomy System for mechanical thrombectomy
Successful revascularization
Defined as proportion of subjects with mTICI 2b-3 flow post treatment with the DAISe Thrombectomy Device.
Time frame: Peri-Procedural
Symptomatic intracranial hemorrhage (sICH) at 24 hours post-procedure
Defined as proportion of subjects with Symptomatic intracranial haemorrhage (sICH) at 24 hours post-procedure as detected by CT/MRI with clinical deterioration of an NIHSS change of greater than or equal to 4.
Time frame: 24 Hours [window: 12-36 hours] post procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.