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Treatment With Endovascular Intervention for STroke Patients With Existing Disability (TESTED)

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University of Cincinnati

Status

Enrolling

Conditions

Stroke
Stroke, Acute
Stroke, Ischemic

Treatments

Procedure: Endovascular Stroke Treatment
Other: Medical Management

Study type

Observational

Funder types

Other

Identifiers

NCT05911568
2023-0299

Details and patient eligibility

About

TESTED will compare the risks and benefits of endovascular thrombectomy (EVT) to medical management (no EVT) in ischemic stroke patients who have a blockage in one of the large blood vessels in the brain and have a moderate-to-severe disability prior to their stroke.

Full description

People with disabilities can suffer acute ischemic stroke (AIS). Endovascular clot removal is a breakthrough therapy for large vessel occlusion (LVO) AIS. Pre-stroke disabled patients were excluded from pivotal EVT stroke trials, so whether EVT is effective for those with pre-stroke disability is not known. As a result, two competing, widely-practiced, treatment paradigms have emerged based on individual practitioners' extrapolation of EVT benefits and safety from patients without a pre-stroke disability to those with disability: 1) Multimodal Medical Management (MMM; using intravenous thrombolysis, antiplatelets, anti-hypertensives, cholesterol lowering medications, and other rehabilitative measures, as indicated) without EVT, and 2) EVT with the background of MMM.

TESTED will enroll patients with LVO-AIS who have a pre-existing disability, defined as pre-stroke modified Rankin score (mRS) 3 and 4, at 12 geographically distinct comprehensive stroke centers serving diverse race-ethnic and socioeconomic populations. The central objective of TESTED is to determine the comparative effectiveness and safety of these two different practice paradigms.

Enrollment

1,060 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult patients (≥18 years)
  2. Moderate-to-severe pre-stroke functional disability, defined as mRS 3-4, for at least 3 months prior to stroke onset
  3. Presenting to study hospital within 24 hours of last known well time
  4. Diagnosis of acute ischemic stroke
  5. Intracranial causative occlusion of the internal carotid artery or the M1 or dominant M2 segments of the middle cerebral artery visualized on the baseline CT(or MR) angiogram
  6. Presenting CT Alberta Stroke Program Early CT (ASPECT) score ≥3 or MRI ASPECT score ≥4
  7. Presenting NIH Stroke Scale score ≥6
  8. Informed consent from patient if competent or from legally authorized representative

Exclusion criteria

  1. Known diagnosis of a terminal cancer or terminal illness at the time of stroke
  2. Assessment of pre-stroke functional status cannot be performed during the hospital stay
  3. Pre-stroke disability deemed temporary in the investigator's opinion (for example, recovering from a general medical illness or traumatic bodily injury)

Trial design

1,060 participants in 1 patient group

Stroke patients with moderate-to-severe pre-stroke disability
Description:
Patients with pre-stroke modified Rankin scale score 3 or 4, presenting with a anterior circulation large vessel occlusion stroke within 24 hours of last known well
Treatment:
Other: Medical Management
Procedure: Endovascular Stroke Treatment

Trial contacts and locations

19

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Central trial contact

Eva Mistry, MD; Naima Griffin

Data sourced from clinicaltrials.gov

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