Stroke Trial, Recruiting NCT07118345 Sponsor: Xuanwu Hospital, Beijing Condition: Stroke
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Stroke Trial, Recruiting

NCT07118345
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 who had little to no disability before their stroke (able to live independently or with minor symptoms beforehand)
  • People where treatment can begin within 24 hours of when they were last known to be well, including strokes noticed upon waking or strokes where no one saw them start
  • People aged 18 to 75 years old
  • People with a confirmed blockage in a specific major brain artery (the internal carotid artery or the main branch of the middle cerebral artery), confirmed by a specialised scan; people with certain nearby artery involvement may also be considered
  • People who show at least some reduced level of alertness that is not caused by brain swelling
  • People whose brain scans show either a very low brain tissue health score (ASPECTS 0–2), or a low score (ASPECTS 3–5) combined with a very high stroke severity score (NIHSS 30 or above)
  • People whose brain scans show that at least half of the middle cerebral artery territory of the brain has been affected by the stroke
  • People with no significant midline shift (the brain has not shifted more than 5mm to one side) on their scan
  • People who have undergone a clot removal procedure (mechanical thrombectomy) with successful restoration of blood flow
  • People where a specific skull surgery (decompressive hemicraniectomy) can be started within 6 hours after the clot removal procedure and within 4 hours after being enrolled in the trial
  • People (or their legal representative) who have given informed consent to participate

Who may not be able to join:

  • People showing signs of brain herniation (such as unequal pupil sizes or unstable vital signs) before being enrolled
  • People where the treating doctor believes life-sustaining care is likely to be withdrawn within the first day
  • People who have already been committed to skull decompression surgery before enrolment
  • People with severely and persistently high blood pressure (systolic above 220 mmHg or diastolic above 110 mmHg)
  • People with blood sugar levels that are very low or very high at the start of the study
  • People with a low platelet count in their blood at the start of the study
  • People with known bleeding disorders, clotting factor deficiencies, or who are on blood-thinning medication with a clotting measurement above a certain level
  • People with severe kidney disease or those already on dialysis
  • People who are unlikely to be able to complete a 90-day follow-up (for example, those without a fixed address or those living overseas)
  • People where vasculitis (blood vessel inflammation) or infection-related clots are suspected as the cause of the stroke
  • People with pre-existing neurological or mental health conditions that would affect assessment of their stroke
  • People who are pregnant or breastfeeding
  • People already participating in another clinical trial that could affect how results are assessed
  • People who, in the treating doctor's judgement, have a life expectancy of less than 3 months due to conditions unrelated to the current stroke, or who are unlikely to follow up as required; other conditions the investigators consider unsuitable or high risk may also apply (confirm with trial site)
  • People with evidence of other existing brain conditions such as a brain injury, brain tumour (except a small, specific type), or brain aneurysm on their scans
  • People with evidence of stroke affecting both sides of the brain's front circulation, or involving the back of the brain (with some specific exceptions)
  • People who experienced a blood vessel injury during the clot removal procedure
  • People whose scans before enrolment show certain types of bleeding in or around the brain; people with only minor or localised bleeding of specific types may still be considered (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 14 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Xuanwu Hospital, Beijing
Registry
ClinicalTrials.gov
Start date
19 July 2025
Est. completion
19 June 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Rate of mRS score of 0-4

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: 14 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