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NCT06194968Recruiting

Treatment of Acute Ischemic StroKe With Intravenous UroKinase Real-world Research: a Multicenter, Prospective Study

Treatment of Acute Ischemic StroKe With Intravenous UroKinase Real-world Research: a Multicenter, Prospective Study (TASK-UK)

Source: ClinicalTrials.gov · Last updated 8 Jan 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to to compare the safety and effectiveness of IV urokinase with IV alteplase in the treatment of AIS in patients up to 6 hours from symptom onset.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1800 (estimated)
First submitted
10 Nov 2023
Start date
30 Dec 2023
Primary completion date
1 Nov 2025
Lead sponsor
The First Affiliated Hospital of Zhengzhou University
Diseases
Stroke
NCT number
NCT06194968

What you commit to

  • Study type: Observational
  • Planned participants: 1800
  • From 30 Dec 2023 to the primary completion date, 1 Nov 2025
  • 16 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

  • Has an expected survival of less than 90 days due to concurrent malignant tumors or severe systemic diseases Incapable to comply with the protocol due to mental illness or cognitive disorder.
  • Paticipants of any interventional drug or device clinical trials within 3 months prior to screening.

Other illness

  • Known history of drug (narcotics, controlled substances) abuse or addiction in the past year.

Other

  • Female of childbearing potential who is known to be pregnant and/or lactating or who has a positive pregnancy test on admission.
  • Unsuitable for this study in the opinion of the investigators.
  • \-

Who the study is looking for

  • First-time occurrence or a history of stroke without significant neurological deficits (baseline mRS score ≤ 1).
  • Eligible for treatment with intravenous administration of urokinase or alteplase as assessed by the investigators.
  • Patient is willing to participate voluntarily and to sign a written patient informed consent. Informed consent will be obtained from each patient or the subject's legally authorized representative or relatives, or deferred where applicable.
  • \-

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

Full criteria on ClinicalTrials.gov

Sites (16)

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

SiteCityCountrySite status
The People's Hospital of Anyang City
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AnyangChinaNot yet recruiting
Beiliu People's Hospital
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BeiliuChinaNot yet recruiting
Guidong People's Hospital of Guangxi zhuang Autonomous Region
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GuidongChinaNot yet recruiting
The First Affiliated Hospital of Jiamusi University
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JiamusiChinaNot yet recruiting
Kaifeng Central Hospital
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KaifengChinaNot yet recruiting
The First People's Hospital of Lanzhou City
Coordinator of this site? Confirm its status
LanzhouChinaNot yet recruiting
The Second People's Hospital of Mengjin District
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LuoyangChinaNot yet recruiting
Pingdingshan The second people's hospital
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PingdingshanChinaNot yet recruiting
Sanya People's Hospital
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SanyaChinaNot yet recruiting
Affiliated Hospital of Inner Mongolia Minzu University
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TongliaoChinaNot yet recruiting
Tengxian People's Hospital
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WuzhouChinaNot yet recruiting
Red Cross Hospital of Yulin City
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YulinChinaNot yet recruiting
The First people's hospital of Yulin
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YulinChinaNot yet recruiting
Affiliated Hospital of Guangdong Medical University
Coordinator of this site? Confirm its status
ZhanjiangChinaNot yet recruiting
The First Affiliated Hospital of Zhengzhou University
Coordinator of this site? Confirm its status
ZhengzhouChinaRecruiting
Huiji District People's Hospital
Coordinator of this site? Confirm its status
ZhengzhouChinaNot yet recruiting

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