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NCT06559241RecruitingPhase 3

Remote Ischemic Conditioning for Acute Ischemic Stroke Treated With Mechanical Thrombectomy(RECAST-MT)

Safety and Efficacy of Remote Ischemic Conditioning for Acute Ischemic Stroke Treated With Mechanical Thrombectomy (RECAST-MT): A Multicenter, Randomized, Controlled, Open-label, Blinded Endpoint Trial

Source: ClinicalTrials.gov · Last updated 10 Dec 2025

Brief summary (registry, in English)

For patients with acute ischemic stroke caused by large vessel occlusion, endovascular thrombectomy has been demonstrated to be the most effective therapy, as approximately 90% of the occluded vessels can be recanalized. However, less than 50% of patients could achieve functional independence, and over 15% died 90 days after stroke. Although the mismatch of successful recanalization with poor prognosis can be attributed to many factors, the infarct core formed during thrombectomy and reperfusion injury after thrombectomy may be among the most important and effective neuroprotective strategies urgently needed. Remote ischemic conditioning (RIC) is a noninvasive strategy in which one or more cycles of brief and transient limb ischemia confer protection against prolonged and severe ischemia in distant organs. In the transient focal cerebral ischemia-reperfusion model, the application of remote ischemic conditioning before reperfusion or both before and after reperfusion reduces reperfusion injuries and the final infarct size. Because patients with acute ischemic stroke who are treated with endovascular thrombectomy can achieve a high rate of recanalization after focal ischemia, this patient population is akin to the model of transient focal cerebral ischemia-reperfusion. Furthermore, a pilot study has determined the safety and feasibility of remote ischemic conditioning in patients undergoing endovascular thrombectomy. However, whether remote ischemic conditioning could provide clinical benefits to patients with acute ischemic stroke who are treated with endovascular thrombectomy urgently needs investigations. This study aims to investigate the safety and efficacy of remote ischemic conditioning in improving functional outcomes of patients with acute ischemic stroke treated with endovascular thrombectomy and explore the effect of treatment duration on the treatment outcome of remote ischemic conditioning.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
2105 (estimated)
First submitted
4 Aug 2024
Start date
23 Sept 2024
Primary completion date
Nov 2026
Lead sponsor
Capital Medical University
Diseases
Stroke
NCT number
NCT06559241

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 2105
  • From 23 Sept 2024 to the primary completion date, Nov 2026
  • 56 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

  • Clinical history, previous imaging examinations, or clinical judgment suggesting intracranial tumors, arteriovenous malformations, or intracranial arterial dissection;

Other illness

  • Difficult-to-control hypertension: continuous monitoring upon admission shows systolic blood pressure ≥180mmHg, or diastolic blood pressure ≥100mmHg;
  • Pre-stroke modified Rankin Scale (mRS) score \>1;
  • Cranial CT or MRI shows intracranial hemorrhage;
  • History of head injury in the past 3 months;
  • History of life-threatening allergy to contrast agents, nickel, titanium metal, or their alloys;
  • Limb deformity, soft tissue injury, or other conditions that affect the implementation of distant ischemia adaptation therapy;
  • Other conditions that the investigators believe are not suitable for participation in this study.

Lab values

  • Presence of bleeding tendency, deficiency of coagulation factors, or oral anticoagulant therapy with INR \> 3.0;
  • Baseline blood glucose \<2.7mmol/L or \>22.2mmol/L;
  • Baseline platelet count \< 30\*10\^9/L;
  • Severe known renal impairment defined as requiring dialysis (hemodialysis or peritoneal dialysis), or if known creatinine clearance rate \<30mL/min;
  • Pregnancy, if women of childbearing age have a positive urinary or serum β-human chorionic gonadotropin (β-hCG) test or are breastfeeding;

Other

  • Imaging examination revealed the presence of multiple vascular supply areas of cerebral infarction (such as the simultaneous presence of infarction in both anterior and posterior circulation);
  • Absence of femoral artery pulsation, extremely difficult intravascular access, or extremely tortuous large vessels, which are expected to result in the inability to undergo timely endovascular treatment;
  • Coma or lethargy patients (consciousness level score ≥2 in NIHSS);
  • Unable to obtain an accurate baseline NIHSS score;
  • Baseline ASPECTS score ≤5;
  • Cranial CT or MRI shows midline deviation and significant occupying effect;
  • The life expectancy of patients is less than 6 months, and they cannot be evaluated within 3 months;
  • Participating in other ongoing clinical trials;

Who the study is looking for

  • Age≥18 years;
  • Acute ischemic stroke due to large vessel occlusion in the anterior circulation that is not suitable for intravenous thrombolytic therapy, or has contraindications to intravenous thrombolytic therapy, or treated with intravenous thrombolytic therapy without recanalization;
  • Large vessel occlusion confirmed by computed tomography angiography (CTA) or magnetic resonance angiography (MRA), including the occlusion of the intracranial segment of the internal carotid artery (ICA) and M1 segment of the middle cerebral artery (MCA), is the cause of symptoms, and mechanical thrombectomy is planned within 24 hours from the time last known well;
  • Baseline score of the National Institutes of Health Stroke Scale (NIHSS) ≥ 6 points;
  • Patients or family members signed a written informed consent form.

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

Full criteria on ClinicalTrials.gov

Sites (56)

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

SiteCityCountrySite status
Anshan Changda Hospital
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AnshanChinaRecruiting
Xuanwu Hospital, Capital Medical University
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BeijingChinaRecruiting
Beijing Fangshan District First Hospital
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BeijingChinaRecruiting
Beijing Daxing District People's Hospital
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BeijingChinaRecruiting
Beijing Luhe Hospital affiliated to Capital Medical University
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BeijingChinaRecruiting
Beijing Red Cross Emergency Medical Center
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BeijingChinaRecruiting
Beijing Chao-Yang Hospital
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BeijingChinaRecruiting
Aerospace Central Hospital
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BeijingChinaRecruiting
Beijing Fengtai You'anmen Hospital
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BeijingChinaRecruiting
Cangzhou Central Hospital
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CangzhouChinaRecruiting
The First People's Hospital of Changde
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ChangdeChinaRecruiting
The Third Xiangya Hospital of Central South University
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ChangshaChinaRecruiting
The First People's Hospital of Chenzhou
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ChenzhouChinaNot yet recruiting
Chongqing University Fuling Hospital
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ChongqingChinaNot yet recruiting
Dalian Central Hospital
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DalianChinaNot yet recruiting
The First Affiliated Hospital of Dalian Medical University
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DalianChinaRecruiting
Shengli Oilfield Central Hospital
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DongyingChinaRecruiting
Fujian Provincial Hospital
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FuzhouChinaNot yet recruiting
Xunxian People's Hospital
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HebiChinaRecruiting
Inner Mongolia Autonomous Region People's Hospital
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HohhotChinaNot yet recruiting
Huanggang Central Hospital
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HuanggangChinaRecruiting
Huangshi Central Hospital
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HuangshiChinaRecruiting
The Hongda Hospital of Jiamusi University
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JiamusiChinaRecruiting
Jiaozuo Coal Industry (Group) Co. Ltd. Central Hospital
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JiaozuoChinaRecruiting
Jinan Third People's Hospital
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JinanChinaRecruiting
Jingmen People's Hospital
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JingmenChinaRecruiting
Jingmen Central hospital
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JingmenChinaRecruiting
Liaocheng People's Hospital
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LiaochengChinaRecruiting
Liaocheng Third People's Hospital
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LiaochengChinaRecruiting
The People's Hospital of Gaotang
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LiaochengChinaRecruiting
Feixian People's Hospital
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LinyiChinaSuspended
Luoyang Yanshi People's Hospital
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LuoyangChinaRecruiting
Mianyang third people's hospital
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MianyangChinaRecruiting
The Second Nanning People's Hospital
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NanningChinaRecruiting
Nanyang Central Hospital
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NanyangChinaRecruiting
South China Hospital Affiliated to Shenzhen University
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ShenzhenChinaRecruiting
Shenzhen Second People's Hospital
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ShenzhenChinaNot yet recruiting
Hebei General Hospital
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ShijiazhuangChinaNot yet recruiting
Army Medical University Noncommissioned Officer School Affiliated Hospital
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ShijiazhuangChinaRecruiting
The First Affiliated Hospital of Soochow University
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SuzhouChinaRecruiting
The Fourth Affiliated Hospital of Soochow University
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SuzhouChinaRecruiting
Suzhou Municipal Hospital of Anhui Province
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SuzhouChinaRecruiting
Taihe County People's Hospital
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Taihe ChengguanzhenChinaRecruiting
First People's Hospital of Tianmen
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TianmenChinaSuspended
Tongling People's Hospital
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TonglingChinaRecruiting
The Second Affiliated Hospital of Wenzhou Medical University
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WenzhouChinaRecruiting
The Third People's Hospital of Hubei Province
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WuhanChinaNot yet recruiting
Zhongnan Hospital of Wuhan University
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WuhanChinaRecruiting
The Central Hospital of Xiangtan
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XiangtanChinaNot yet recruiting
Ya 'an People's Hospital
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Ya'anChinaRecruiting
YEDA hospital
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YantaiChinaRecruiting
Yichang Central People's Hospital
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YichangChinaRecruiting
Yueqing People's Hospital
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YueqingChinaRecruiting
Zhangzhou Municipal Hospital of Fujian Province
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ZhangzhouChinaRecruiting
Henan Province People's Hospital
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ZhengzhouChinaNot yet recruiting
Xihua County People's Hospital
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ZhoukouChinaRecruiting

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