NCT06870448Not yet recruitingPhase 3
Methylprednisolone With Endovascular Thrombectomy for Large Ischemic Stroke
Methylprednisolone With Endovascular Thrombectomy for Large Ischemic Stroke (MATCH): A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 11 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
It is uncertain whether intravenous methylprednisolone improves outcomes for acute anterior circulation large vascular occlusion (LVO) patients with a large infarct core. In this study, the investigators assume that methylprednisolone plus endovascular thrombectomy (EVT) might be superior to EVT alone for patients who have evidence of a large infarct volume. The objective of the study was to establish the efficacy and safety of methylprednisolone with EVT in patients presenting with symptoms of acute ischemic stroke from LVO in the anterior circulation and having a large infarct volume.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 1614 (estimated)
- First submitted
- 6 Mar 2025
- Start date
- Apr 2025
- Primary completion date
- Jan 2029
- Lead sponsor
- Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
- Diseases
- Stroke
- NCT number
- NCT06870448
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 1614
- From Apr 2025 to the primary completion date, Jan 2029
- 1 site 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.
Other illness
- 1\. Intracranial hemorrhage confirmed by CT or MRI;
- 2\. Allergic to glucocorticoids or placebo components;
- 3\. Allergic to contrast agent;
- 4\. Presence of severe infectious disease unsuitable for glucocorticoid therapy or any other contraindication to glucocorticoid use;
- 8\. History of gastrointestinal or urinary tract bleeding within the last month;
- 12\. Uncontrolled hypertension with persistent systolic blood pressure \>185 mmHg or diastolic blood pressure \>110 mmHg, refractory to medical management;
- 13\. Life expectancy less than 6 months due to malignancy or severe cardiopulmonary disease;
- 14\. Other conditions deemed unsuitable for the study by the investigator, such as inability to comprehend or comply with study procedures or follow-up due to mental illness, cognitive or emotional disorder.
Lab values
- 5\. Known genetic or acquired coagulopathy, coagulation factor deficiency, use of warfarin with an international normalized ratio (INR) \>1.7, or use of novel oral anticoagulants within 48 hours of symptom onset;
- 6\. Platelet count \<90×10\^9/L;
- 7\. Random blood glucose \<2.8 mmol/L or \>22.2 mmol/L;
- 11\. Renal dysfunction (glomerular filtration rate \<30 ml/min or serum creatinine \>220 μmol/L \[2.5 mg/dl\]);
Other
- 9\. Current participation in another interventional clinical study;
- 10\. Pregnant or lactating women;
Who the study is looking for
- 1\. Age ≥18 years;
- 2\. Clinically diagnosed with acute ischemic stroke and NIHSS ≥6;
- 3\. CT angiography (CTA), MR angiography (MRA) or digital subtraction angiography (DSA) confirmed occlusion of intracranial internal carotid artery (ICA) or M1/M2 segments of middle cerebral artery (MCA) and plan to undergo EVT;
- 4\. ASPECTS ≤5 (based on NCCT) or infarct core volume ≥70mL (defined as rCBF \<30% on CT perfusion or ADC \<620 on MRI);
- 5\. Time from symptom onset to randomization within 24 hours (from last known well);
- 6\. Pre-stroke mRS score 0-2;
- 7\. Written informed consent signed by patients or their family members.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sun Yat-sen Memorial Hospital, Sun Yat-sen University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.