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临床试验/NCT04588337
NCT04588337已完成不适用

INtravenous TNK for Acute isChemicsTroke in China (INTACT-China): a Prospective, Multi-center, Registry Study

General Hospital of Shenyang Military Region1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2022年1月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,000
试验地点
1
主要终点
The proportion of excellent prognosis (mRS 0-1)

研究概览

简要总结

Acute ischemic stroke is the most common type of stroke, accounting for about 60%-80% of all stroke, with high incidence, high mortality, high disability rate, has become the first cause of death in China. At present, only ultra-early thrombolytic therapy, endovascular therapy and antiplatelet therapy have obtained evidence-based medical evidence in ischemic stroke treatment, but only thrombolytic therapy and endovascular therapy can improve the good prognosis of patients. Intravenous thrombolytic therapy within 4.5 hours after the onset of ischemic stroke symptoms has been shown to be effective, which is recommended in the guidelines.

In most countries, alteplase (R-tPA) is the only drug approved for the treatment of acute ischemic stroke. Recombinant human TNK tissue-type plasminogen activator (rhTNK-tPA) is a modified recombinant tissue-type plasminogen activator, with no procoagulant effect and a longer half life. In recent years, there are some studies on the comparison of therapeutic effects of TNK-tPA and RT-PA in patients with acute ischemic stroke, and TNK shows promising especially for large artery occlussion. At present, there are few reports on the application of rhTNK-tPA in Chinese stroke patients.

The aim of this study is to evaluate the efficacy and safety of rhTNK-tPA in Chinese patients with ischemic stroke in a prospective, multicenter registration study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • The time from onset to treatment was less than 4.5 hours;
  • Ischemic stroke confirmed by head CT or MRI;
  • There are measurable neurological deficits;
  • First onset or previous onset without obvious sequelae (Mrs ≤1 score) ;
  • signed informed consent.

排除标准

  • Severe neurologic deficits before onset (mRS ≥2) ;
  • Significant head trauma or stroke in the last 3 months;
  • Subarachnoid hemorrhage;
  • A history of intracranial hemorrhage or head injury or acute stroke within 3 months;
  • Intracranial tumors, arteriovenous malformations or aneurysms;
  • Intracranial or spinal cord surgery within 3 months;
  • Non-compressible arterial puncture within 7 days;
  • Gastrointestinal or urinary tract hemorrhage within last 21 days;
  • Major surgery within 1 month;
  • Thrombocytopenia (platelet count <10×109/L);
  • Use of heparin or oral anticoagulation therapy within 48 hours;
  • Use of warfarin with an international normalised ratio >1.7 or PT >15 s;
  • Uncontrolled hypertension (SYSTOLIC >180 mmHg OR DIASTOLIC>110 mmHg) ;
  • The Blood Glucose concentration <50 mg/dl (2.7 mmol/L);
  • Severe systemic disease with poor life expectancy (<3 months); ;
  • Allergic to research drug;
  • Within 3 months or participating in other clinical trials;
  • Other conditions due to which investigators consider study participation inappropriate.

结局指标

主要结局

The proportion of excellent prognosis (mRS 0-1)

时间窗: 90 ± 7 days

The proportion of excellent prognosis (mRS 0-1) after thrombolysis

次要结局

  • symptomatic intracerebral hemorrhage(within 36 hours)
  • the proportion of good prognosis (mRS 0-2)(90 ± 7 days)
  • The incidence of stroke deterioration after thrombolysis(within 1 week)
  • the incidence of stroke recurrence and other vascular events(within 90 ± 7 days)

研究者

发起方
General Hospital of Shenyang Military Region
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hui-Sheng Chen

Head of Neurology

General Hospital of Shenyang Military Region

研究点 (1)

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