Stroke Trial, Recruiting NCT07047326 Sponsor: Capital Medical University Condition: Stroke
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Stroke Trial, Recruiting

NCT07047326
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 to 80 years, of any gender
  • People who have been clinically diagnosed with an ischemic stroke (a stroke caused by a blockage), following recognised Chinese stroke diagnosis guidelines
  • People where treatment can begin within 6 hours of when symptoms first started, where symptoms have lasted at least 30 minutes and have not significantly improved before treatment
  • People who show at least some measurable stroke symptoms at the start of the trial, as assessed by a standard medical scale (NIHSS score of 1 or more)
  • People, or their legal guardians, who are willing to sign a consent form agreeing to take part

Who may not be able to join:

  • People whose brain scan (CT or MRI) shows a large area of damage covering more than one-third of a specific brain artery's territory (the middle cerebral artery)
  • People where the exact time their stroke symptoms began is not known
  • People who already had some level of disability before the stroke, based on a standard disability scale (pre-stroke mRS score of 2 or higher)
  • People with a significantly reduced level of consciousness, as measured by a specific part of the stroke assessment scale (NIHSS item 1A score of 2 or more)
  • People who have any bleeding inside the skull, such as a brain bleed, bleeding into fluid-filled spaces, bleeding around the brain, or bleeding between the skull and brain
  • People with a previous history of bleeding inside the skull
  • People with a tendency to bleed easily, including those with a low platelet count (below 100 × 10⁹/L) or other bleeding-related conditions
  • People who have received heparin (a blood-thinning medication) within the past 24 hours
  • People taking oral blood-thinning medications (such as warfarin) whose blood test results show their blood is thinning more than a certain level (INR above 1.7 or PT above 15 seconds)
  • People who have had, or are planned to have, a procedure to treat the stroke from inside the blood vessels (endovascular therapy)
  • People who have had a serious head injury or stroke within the past 3 months
  • People with a tumour inside the skull or a large brain aneurysm (a bulge in a blood vessel in the brain)
  • People who have had surgery inside the skull or on the spine within the past 3 months
  • People who have had a major surgical procedure within the past 2 weeks
  • People with serious liver disease, such as liver failure, cirrhosis, high blood pressure in the liver's blood vessels, or active hepatitis
  • People who have had bleeding in the stomach, intestines, or urinary tract within the past 3 weeks
  • People who currently have active bleeding inside the body
  • People found to have a tear in the main large blood vessel from the heart (aortic dissection)
  • People who have had a needle inserted into an artery in a location that is difficult to apply pressure to, within the past week
  • People who are not expected to survive beyond one year due to other serious health conditions
  • People with very high blood pressure that cannot be controlled even with medication — specifically, a top reading at or above 180 mmHg or a bottom reading at or above 100 mmHg, confirmed across three separate measurements taken 10 minutes apart
  • People whose blood sugar level is very low (below 2.8 mmol/L) or very high (above 22.2 mmol/L)
  • People who are unable or unwilling to participate due to a seizure-related weakness, or due to other neurological or psychiatric conditions
  • People with a known allergy to urokinase (the medication being studied)
  • People with a bacterial infection of the heart lining, inflammation around the heart, or acute inflammation of the pancreas
  • People who have taken part in another clinical trial within the 30 days before being assessed for this trial
  • People who are pregnant, breastfeeding, or not willing to use effective contraception during the trial
  • People who the trial investigator considers unsuitable for any other reason that may affect their safety or ability to follow the trial requirements

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 010-8319-9439

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Capital Medical University
Registry
ClinicalTrials.gov
Start date
1 October 2025
Est. completion
2 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of participants with major response

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov