Phase 3 Stroke Trial, Recruiting NCT07135089 Sponsor: General Hospital of Shenyang Military Region Condition: Stroke
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Phase 3 Stroke Trial, Recruiting

NCT07135089
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 or older
  • People who have a confirmed blockage in a major blood vessel supplying the front part of the brain (specifically the internal carotid artery or a main branch of the middle cerebral artery), confirmed by a specialised type of scan (CTA or MRA)
  • People for whom a procedure to remove the blood clot is considered appropriate within 12 hours of symptoms starting
  • People whose stroke is strongly suspected to be caused by a build-up of fatty deposits (plaque) in the arteries, based on their medical history, symptoms, and scan results
  • People with a stroke severity score of 6 or higher on a standard medical scale (NIHSS) at the start
  • People whose brain scan shows a score of 6 or higher on a measure of how much brain tissue is still healthy (ASPECTS)
  • People who were largely independent in daily life before the stroke (a functional score of 2 or less on a standard scale called the mRS)
  • People (or their legal representative) who have signed a consent form agreeing to take part

Who may not be able to join:

  • People who have a history of irregular heart rhythms called atrial fibrillation or atrial flutter, or whose heart tracing (ECG) shows these rhythms after admission
  • People who have had a bleeding-type stroke (such as a brain bleed or bleeding around the brain), or any bleeding event in the past month
  • People who have brain aneurysms, abnormal blood vessel formations in the brain, very twisted arteries that would make the clot-removal procedure difficult, or brain tumours that are causing pressure in the skull
  • People who have taken certain blood-thinning or antiplatelet medications in the past week, including dual antiplatelet therapy, direct oral anticoagulants, or warfarin
  • People with severely uncontrolled high blood pressure (top number above 200 mmHg or bottom number above 110 mmHg)
  • People with certain blood clotting problems, a key clotting measurement (INR) above 1.7, or a low platelet count (below 90×10⁹/L)
  • People with severe kidney problems or a serious illness where life expectancy is less than 6 months
  • People who are pregnant or breastfeeding
  • People with known allergies to medications or contrast dyes used in scans
  • People already taking part in another clinical trial
  • People whom the research team considers unsuitable for other reasons (confirm with trial site)

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 9 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: +86-024-28897511

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
General Hospital of Shenyang Military Region
Registry
ClinicalTrials.gov
Start date
13 November 2025
Est. completion
30 September 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The proportion of patients with functional independence (modified Rankin Scale [mRS] score of 0 to 2)

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: 9 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