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Optical Coherence Tomography Guided Antithrombotic Treatment After Endovascular Thrombectomy of the Posterior Circulation

Optical Coherence Tomography Guided Antithrombotic Treatment After Endovascular Thrombectomy of the Posterior Circulation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04121611
Enrollment
25
Registered
2019-10-10
Start date
2019-10-14
Completion date
2021-12-14
Last updated
2019-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke of Basilar Artery, Optical Coherence Tomography, Antithrombotics, Endovascular Thrombectomy

Keywords

Basilar, Stroke, Thrombus, Optical Coherence Tomography

Brief summary

Evidence regarding the role of early (\<24 hours) antithrombotics post-revascularization with either intravenous thrombolysis (IVT), endovascular thrombectomy (EVT), or a combination of both remains scarce. In 2018 the American Heart Association/American Stroke Association changed their recommendation, stating that the risk of antithrombotic therapy within the first 24 hours after treatment with IVT (with or without EVT) is uncertain. This was changed after data emerged that early antithrombotics may be safe and may improve outcomes in select patients undergoing EVT. Recently the investigators showed for the first time that significant residual basilar thrombus can exist after EVT despite complete angiographic revascularization using endovascular optical coherence tomography imaging. This residual thrombus could cause ongoing function-limiting strokes with occlusion of vital basilar perforators after EVT. Therefore, the investigators propose a prospective,non-randomized safety study to evaluate optical coherence tomography guided antithrombotic management for patients with confirmed residual thrombus after EVT for basilar occlusion.

Interventions

1. Acetylsalicylic Acid (ASA) 325mg PO/PR/NG loading dose \< 2 hours of EVT completion 2. ASA 81mg PO OD maintenance dose

DRUGUnfractionated heparin

1. Intravenous unfractionated heparin (UFH) infusion within 6 hours of EVT with target activated partial thromboplastin time (aPTT) 64-86 2. Anticoagulation to continue for minimum of 48 hours (can be maintained on UFH aPTT 64-86 or transitioned to low-molecular weight heparin (LMWH) Enoxaparin 1mg/kg)

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- All patients deemed candidates for endovascular thrombectomy(EVT) for basilar artery occlusion. As no robust guidelines exist for the role of EVT in patients with acute basilar artery occlusion, the decision for EVT is made by a team of stroke neurologist and neuro-interventionalist at our regional stroke center.

Exclusion criteria

* High-density lesion consistent with hemorrhage of any degree. * Significant established infarct size. * Contraindication to receiving post-revascularization antithrombotics for any reason (history of major hemorrhage in the past six months, hereditary or acquired bleeding diathesis, major surgery within last three months, platelets \<100 X 109 /L, coagulation factor deficiency, already on anticoagulant that would not allow administration of UFH) * Informed consent is not or cannot be obtained. * Females of childbearing potential who are known to be pregnant and/or lactating or who have positive pregnancy tests on admission. * Other serious, advanced, or terminal illness. * Patients who require hemodialysis or peritoneal dialysis. * Uncontrolled hypertension defined as systolic blood pressure\>185 mm Hg or diastolic blood pressure\>110mm Hg that cannot be controlled except with continuous parenteral antihypertensive medication

Design outcomes

Primary

MeasureTime frameDescription
Favorable outcome90 daysFavorable outcome at day 90 defined as a modified Rankin Score (mRS - functional scale) of 0-3.

Secondary

MeasureTime frameDescription
Symptomatic Intracranial Hemorrhage24 hours CT imaging ± 8 hours.
Incidence of residual thrombusImmediately after endovascular thrombectomyFraction of patients with residual thrombus after endovascular thrombectomy as observed with optical coherence tomography
Excellent Outcome90 daysExcellent outcome at day 90 defined as a modified Rankin Score (mRS - functional scale) of 0-2.

Countries

Canada

Contacts

Primary ContactChristopher R Pasarikovski, MD
chris.pasarikovski@mail.utoronto.ca647-550-0862
Backup ContactVictor XD Yang, MD
victor.yang@sunnybrook.ca416-480-6100

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026