Clinical Trial Details
— Status: Withdrawn
Administrative data
NCT number |
NCT03176420 |
Other study ID # |
UIHC |
Secondary ID |
|
Status |
Withdrawn |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
March 1, 2020 |
Est. completion date |
March 31, 2023 |
Study information
Verified date |
May 2023 |
Source |
University of Iowa |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This is a phase 2 randomized single-center open label clinical trial with randomization of
1:1 to either best medical management vs. best medical management and endovascular
revascularization of chronically occluded ICA (COICA). The study will utilize best medical
management and will randomize patients to endovascular balloon angioplasty and stenting.
Primary Objective:
To test the hypothesis that endovascular revascularization of COICA improves significantly
cognitive function assessed by a specifically designed battery of 14 cognitive tests
including the Montreal Cognitive Assessment (MoCA).
Secondary Objective:
To test the safety of endovascular revascularization of chronically occluded ICA.
Tertiary/exploratory Objectives:
To test the hypothesis that subjects with symptomatic COICAs and mild/moderate cognitive
dysfunction have the following biomarkers:
A) Presence of lactate and decreased Naa/Cr in the watershed area (specifically centrum
semiovale) on 1H-MRI-spectroscopy, and B) Decreased size of the hippocampus and amygdala on
MRI. C) increased MTT on CTP in the ipsilateral side of the occluded ICA specifically in the
MCA territory when compared to the opposite unaffected hemisphere.
Description:
Background:
Complete occlusion of the internal carotid artery (COICA) by atherosclerotic disease causes
approximately 15%-25% of ischemic strokes in the carotid artery distribution. Patients
treated with medical therapy have 5%-8% risk per year for ipsilateral ischemic stroke during
the first 2 years after internal carotid artery occlusion. Internal carotid artery occlusion
causes an estimated 61,000 first-ever strokes per year in the USA, an incidence more than
twice the annual occurrence of ruptured intracranial aneurysms. Additionally, 40% of subjects
with COICA who present with transient ischemic attacks (TIA) and 70% of COICA who present
with stroke have cognitive decline with significantly increased risk of vascular dementia and
Alzheimer's' disease (AD) with time 2,3.
Our group and others have used an alternative approach to revascularize subjects with COICAs.
These studies showed the feasibility and safety of using endovascular angioplasty and
stenting (EAS) and/or hybrid of both carotid endarterectomy (CEA) and EAS to restore cerebral
flow to the ipsilateral hemisphere of the COICA. A meta-analysis of these studies, identified
333 subjects with COICA, an average age of 67.2 ± 9.3 years, and a male proportion of 85%.
The average known occlusion time was 8.8 ± 10.0 months. Successful revascularization was
achieved in 70% (232/333), with major complications found in 13 (3.9%) subjects and minor
complications in 8 (2.4%) subjects. Furthermore, our group devised a new angiographic and
anatomic classification to upfront predict the success of revascularization using these
techniques. This classification was tested in 2 pilot studies and the results showed robust
plausibility to predict upfront the percentage of success anticipated in revascularizing
these lesions using these techniques. In addition, 3 groups including ours showed that
revascularization using these techniques restored cerebral blood flow to the ipsilateral
hemisphere of the COICA evident of normalization of mean transient time (MTT) on CT perfusion
(CTP) and significant improvement in the cognitive function. Previous attempts to improve
cognitive function in this cohort failed using bypass (COSS Trial).The rationale for failure
is the fact that this technique relied on a very small caliber donor artery (STA) to
revascularize the entire hemisphere affected. This significantly improved the oxygen
extraction in the middle cerebral artery territory affected but failed to normalize it.
Additionally, this technique provided cerebral flow to majority of ipsilateral middle
cerberal artery territory but not enough to vascularize the Anterior cerebral artery
territory, which supplies the majority of the limbic system involved in executive and
cognitive functioning. EAS and hybrid technique restore the caliber of the cervical internal
carotid arteryand therefore, the blood flow to all involved vessels (anterior and middle
cerebral artery, and other branches) with clear evidence of complete resolution of penumbra
and normalization of MTT on CTP. This could provide an explanation of the difference of both
techniques in improving cognitive function.
All subjects who presents to our tertiary hospital with a diagnosis of COICA will undergo
full evaluation including 1) documenting previous history of TIA and/or stroke; 2) cervical
and brain CTA to document complete occlusion; 3) CTP to assess for presence of penumbra
evident by increased MTT in the ipsilateral side of COICA; and 4) MoCA. If any subject is
found to have complete occlusion of COICA, evident of abnormal/prolongation of MTT on CTP,
previous history of TIA and or stroke, and MoCA <26 & ≥ 23, then further evaluation is
obtained including: 1H-MRI spectroscopy to assess for presence/absence of lactate in the
ipsilateral watershed area (centrum semiovale), ratio of Naa/Cr, and size of ipsilateral
hippocampus and amygdala, additional cognitive testing battery, and DSA to document
adequately the type of COICA the subject have (type A-D).
If any subject does not have complete occlusion, or complete occlusion but no abnormalities
on CTP and/or MoCA >26, then the subject is excluded and no further testing needed (see
exclusion criteria).
If the subject meets all inclusion criteria, then a baseline of complete neurological
testing, full demographics, CTA or MRA, CTP, MoCA, additional neurological testing (see
below), 1H-MRI sectroscopy and DSA are obtained and subject is randomized 1:1 to either best
medical management or best medical management + endovascular balloon angioplasty and
stenting. Follow up clinic visits are arranged at 3 and 12 months. Repeat testing of MoCA and
additional cognitive testing battery are done at these clinical follow-up visits (3 and 12
months). MRI of the brain and DSA is performed at 1 year follow-up to assess brain biomarkers
and revascularization respectively.