The Correlation of Intracranial Artery Calcification and Outcomes of Mechanical Thrombectomy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorZhujiang Hospital

About this trial

CAIS-MT is a single-center, prospective cohort study, to evaluate the correlation between outcomes of endovascular treatment(EVT) and intracranial artery calcification(IAC) in patients with acute ischemic stroke due to large or medium vessel occlusion.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or non-pregnant women with acute stroke symptoms aged over 18 years.

Occlusion of the intracranial internal carotid artery, the middle cerebral artery, the anterior cerebral artery, the posterior cerebral artery, basilar artery and intracranial vertebral artery confirmed by CT, MR angiography, or digital subtraction angiography.

No absolute contraindication to iodinated contrast media.

Planned treatment with EVT by clinical care team.

Disqualifiers

Acute ischemic stroke occurs over 24 hours of time last known well.

Neurologic deficits caused by diagnoses other than ischemic stroke, such as intracerebral hemorrhage, subarachnoid hemorrhage, or intracranial tumors.

With other underlying factors leading to IAC, such as hyperthyroidism, end-stage renal disease, long-term oral intake of vitamin K antagonist(Warfarin), chronic vitamin D deficiency or overdose, persistent hypomagnesemia, persistent hypercalcemia, persistent hyperphosphatemia and high oral calcium intake.

Lack of non-contract CT images on admission and significant artifacts in CT images preventing IAC measurement.

Trial population

Patients with a diagnosis of acute ischemic stroke due to large or medium vessel occlusion, who are enrolled at Zhujiang Hospital and meet the indication for EVT.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

434 Participants
are grouped into 1 trial group
Group A: Patients with acute ischemic stroke due to large or medium vessel occlusion

Trial outcomes

Primary outcomes

1

Proportion of patients with a adverse functional outcome at 3 months

Modified Rankin Scale(mRS) score \> 2

Time frame
90(±7) days

Secondary outcomes

1

Proportion of patients without disability at 3 months

mRS score 0-1

Time frame
90(±7) days
2

Proportion of patients with functional independence at 3 months

mRS score 0-2

Time frame
90(±7) days
3

Proportion of patients ambulatory or bodily needs-capable or better at 3 months

mRS score 0-3

Time frame
90(±7) days
4

Change of the NIHSS score at 24 hours from baseline

Change of the NIHSS score at 24 hours from baseline

Time frame
24 hours

Other outcomes

Sponsors and contacts

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