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NCT07185022Recruiting

Intra-arterial Thrombolysis for Acute Ischemic Stroke With Medium Vessel Occlusion

a Multicenter Prospective Randomized Controlled Trial of Intra-artErial thrombolysiS for aCUte Ischemic strokE With Medium Vessel Occlusion (RESCUE MeVO)

Source: ClinicalTrials.gov · Last updated 16 Apr 2026

Brief summary (registry, in English)

Acute ischemic stroke (AIS) due to medium vessel occlusion (MeVO) or severe stenosis poses a significant clinical challenge. Recent large randomized controlled trials, DISTAL and ESCAPE-MeVO, demonstrated no significant benefit of endovascular therapy in patients with MeVO. Although intra-arterial thrombolysis has shown promise in clinical experience, robust evidence supporting its efficacy in MeVO or severe stenosis-related AIS is still absent. To fill this gap, the RESCUE MeVO trial has been designed as a multicenter, prospective, randomized, open-label, blinded end-point (PROBE) study to evaluate the efficacy and safety of intra-arterial thrombolysis in patients with AIS caused by MeVO or severe stenosis.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
282 (estimated)
First submitted
15 Sept 2025
Start date
6 Jan 2026
Primary completion date
1 Feb 2030
Lead sponsor
The Second Hospital of Anhui Medical University
Diseases
Stroke
NCT number
NCT07185022

What you commit to

  • Study type: Interventional
  • Planned participants: 282
  • From 6 Jan 2026 to the primary completion date, 1 Feb 2030
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Secondary MeVO or severe stenosis caused by endovascular therapy

Other illness

  • Pre-stroke mRS ≥ 2
  • Neuroimaging demonstrated intracranial hemorrhage, subarachnoid hemorrhage, or other hemorrhagic disorders
  • Persistent and uncontrolled hypertension, defined as systolic blood pressure \>185 mmHg or diastolic blood pressure \>110 mmHg
  • History of intracranial hemorrhage within the past 3 months, including parenchymal hemorrhage, intraventricular hemorrhage, subarachnoid hemorrhage, epidural hemorrhage, or subdural hemorrhage
  • Gastrointestinal or urinary tract bleeding, or major surgery within the past 3 months
  • Patients with known allergy to thrombolytic agents or their excipients
  • Patients with known allergy to iodinated contrast agents or other established contraindications

Lab values

  • Platelet count \<100 × 10⁹/L, known bleeding tendency or coagulation factor deficiency, or oral anticoagulant therapy with an international normalized ratio (INR) \>3.0
  • Chronic dialysis or severe renal impairment, defined as a glomerular filtration rate (GFR) \<30 mL/min or serum creatinine \>220 μmol/L (2.5 mg/dL)

Other

  • Non-contrast CT demonstrating a clearly hypodense lesion corresponding to the vascular territory
  • Presence of arteriovenous malformations or brain tumors with mass effect
  • Pregnant or current breastfeeding
  • Presence of severe systemic comorbidities with a life expectancy of less than 3 months
  • Deemed unsuitable for participation by the investigator for any reason

Who the study is looking for

  • Age \> 18 years
  • Primary medium vessel occlusion (MeVO) or severe stenosis (≥70%) was detected on CTA, MRA, or DSA, involving arterial segments including M2-M3 of the middle cerebral artery (MCA), A1-A2 of the anterior cerebral artery (ACA), P1-P2 of the posterior cerebral artery (PCA), and the anterior inferior cerebellar artery (AICA), posterior inferior cerebellar artery (PICA), and superior cerebellar artery (SCA)
  • The clinical symptoms were consistent with MeVO, with a NIHSS score 5 - 25, or an NIHSS score of 3-4 in the presence of disabling neurological deficits (e.g., hemianopia, aphasia, or motor dysfunction)
  • Intra-arterial thrombolysis was administered within the following time windows:
    • Acute ischemic stroke within 24 hours of symptom onset or last known well, including stroke with known onset, wake-up stroke and stroke with unknown onset, with no obvious hypodensity on CT and good collateral circulation on CTA;
    • Acute ischemic stroke within 24-72 hours of onset, meeting at least one of the following imaging criteria: a.CT or MR perfusion imaging demonstrating target mismatch, defined as an ischemic core volume \<30 mL, a mismatch ratio ≥1.2, and a mismatch volume ≥10 mL.; b.MRI demonstrating DWI-FLAIR mismatch, defined as the presence of acute ischemic lesions on diffusion-weighted imaging (DWI) with no corresponding hyperintense signal on FLAIR, or with FLAIR hyperintense lesions occupying less than one-third of the DWI lesion volume.
  • Signed informed consent obtained

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lin Quan People's Hospital
Coordinator of this site? Confirm its status
FuyangChinaRecruiting
Fu Yang People's Hospital
Coordinator of this site? Confirm its status
FuyangChinaRecruiting
The Second Affiliated Hospital Of Anhui Medical University
Coordinator of this site? Confirm its status
HefeiChinaRecruiting
Lishui Central Hospital
Coordinator of this site? Confirm its status
LishuiChinaRecruiting
Liuzhou Worker's Hospital
Coordinator of this site? Confirm its status
LiuzhouChinaRecruiting
Shucheng People's Hospital
Coordinator of this site? Confirm its status
Lu'anChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.