Phase 3 Stroke Trial, Recruiting NCT07379190 Sponsor: Weifang Medical University Condition: Stroke
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Phase 3 Stroke Trial, Recruiting

NCT07379190
Recruiting Phase 3

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 years or older.
  • People who have had an acute ischemic stroke (a stroke caused by a blocked blood vessel) in a specific part of the brain's blood supply, confirmed by symptoms and medical imaging.
  • People whose stroke symptoms started, or who were last known to be well, more than 24 hours but no more than 7 days before joining the trial.
  • People whose stroke has been confirmed through specialised brain vessel imaging to be caused by a narrowing or hardening of arteries inside the skull, with other causes such as heart-related clots ruled out.
  • People whose stroke severity falls within a specific moderate range on a standard medical scoring scale at the time of joining (confirm with trial site).
  • People, or their legal representative, who have signed a consent form agreeing to take part.

Who may not be able to join:

  • People who are planned to receive clot-dissolving treatment (either through a vein or a procedure inside a blood vessel).
  • People with bleeding inside the brain confirmed by a CT scan.
  • People whose stroke is confirmed or suspected to have been caused by a clot travelling from the heart.
  • People with a history of atrial fibrillation (an irregular heart rhythm), or whose current heart tracing shows atrial fibrillation.
  • People whose stroke was caused by other specific conditions such as Moyamoya disease, a torn artery wall, or inflamed arteries.
  • People whose brain imaging shows the area of stroke damage covers more than half of a single brain lobe.
  • People who have a known reason why antiplatelet medicines (blood-thinning tablets such as aspirin) cannot be used, including bowel bleeding, stomach or gut bleeding, or other bleeding conditions.
  • People with a known allergy or sensitivity to aspirin.
  • People who are expected to need blood-thinning (anticoagulant) medication during the trial for conditions such as atrial fibrillation, a mechanical heart valve, blood clots in the legs or lungs, or related conditions.
  • People with certain serious health conditions including cancer, regular kidney dialysis, severely reduced kidney function, or severely reduced liver function (confirm with trial site for specific test values).
  • People with severe heart failure classified as Class III or IV on a standard medical scale.
  • People with a serious non-heart-related illness where survival is estimated at less than 6 months.
  • People who have had a new stroke affecting both the front and back areas of the brain's blood supply at the same time.
  • People who are not able to complete the required follow-up appointments and assessments.
  • People with other known neurological (brain or nerve) conditions that may affect follow-up results.
  • People who are currently taking part in another treatment-based clinical trial that has not yet been completed.
  • People whom the trial doctors consider unsuitable for other reasons.

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 15 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 86-0536-8192680

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

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Weifang Medical University
Registry
ClinicalTrials.gov
Start date
22 June 2026
Est. completion
1 February 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Proportion of participants with functional independence outcome [modified Rankin Scale(mRS) score 0-1]

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: 15 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