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NCT07519889Possibly a fitNot yet recruiting

Comparing the safety of two clot-dissolving drugs for acute ischemic stroke

Acute Ischemic StrokerhTNK-tPA

Treatments studied

Part of Brain & nervous system, Heart & circulation clinical trials.

This study compares the safety of two clot-dissolving drugs, rhTNK-tPA (Mingfule) and rt-PA (Actilyse), for treating acute ischemic stroke. It aims to see if the newer drug (Mingfule) is as safe as the standard one (Actilyse) when given within 4.5 hours of stroke onset.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
4,500 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be 18 years or older
  • You must have had a stroke due to a blocked blood vessel, confirmed by a CT or MRI scan
  • You need to start treatment within 4.5 hours from when your symptoms began (or when you were last seen normal)
  • Your stroke severity must be mild to moderate (on a standard scale of 0-42, you must score 25 or less)
  • You cannot have any major bleeding risks, such as recent surgery, bleeding in the stomach or brain, or untreated high blood pressure
  • You must not have already received a clot-dissolving drug or a clot-removal procedure before arriving at the study hospital

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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