Stroke Trial, Recruiting NCT06472336 Sponsor: University Hospital, Basel, Switzerland Condition: Stroke
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Stroke Trial, Recruiting

NCT06472336
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 are 18 years of age or older
  • People who have had a stroke with a significant level of disability, measured by a standard stroke severity scoring tool (a score of 6 or more for strokes affecting the front of the brain, or 10 or more for strokes affecting the back of the brain)
  • People where it is expected that they can be enrolled in the trial within 24 hours of when they were last known to be well
  • People who have a blockage in one of several specific large blood vessels in the brain (the internal carotid artery, certain parts of the middle cerebral artery, the basilar artery, or a specific section of the vertebral artery)
  • People whose blocked blood vessel has not reopened after up to three attempts at mechanical clot removal during a procedure to treat the stroke
  • People where the treating doctor believes there is a high likelihood that the blockage is caused by hardening and narrowing of the arteries inside the brain (a condition called intracranial atherosclerotic disease)
  • People whose blocked artery the treating doctor considers suitable for placement of a stent
  • People who do not have a very large area of permanently damaged brain tissue, as assessed by a standard brain scan scoring method (a score of 6 or above on a specific scale used for strokes at the back of the brain)
  • People who have given informed consent by signing the relevant forms, or where emergency consent procedures have been followed

Who may not be able to join:

  • People who have active bleeding inside the brain
  • People who had significant disability before the stroke, defined as a score of 3 or above on a standard disability scale
  • People with serious known health conditions that would likely prevent recovery or attendance at follow-up appointments, such as cancer, dementia, or significant alcohol or drug misuse
  • People with a known blood clotting disorder, or where an underlying condition causing the blood to clot too easily is suspected
  • People whose stroke occurred while they were already in hospital
  • People with known reasons why blood-thinning (anti-platelet) medications cannot be used
  • People with a known serious allergic reaction to contrast dye used in imaging, or to nickel, titanium, or related metals (which may be present in a stent)
  • People where attending follow-up appointments is unlikely to be possible due to geographic reasons, such as living overseas
  • People who are known to be pregnant at the time of enrolment
  • People whose brain scans show evidence of significant brain swelling caused by a mass, or a brain tumour (except for a small, non-concerning type called a meningioma)
  • People whose brain scans show evidence of inflammation of blood vessels in the brain (cerebral vasculitis)
  • People whose blocked blood vessel has already reopened before enrolment into the trial
  • People who are already participating in another interventional clinical trial that could affect the results of this study

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 7 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

Principal Investigator: Marios-Nikos Psychogios, Prof. Dr., University Hospital, Basel, Switzerland

Phone: +41 76 233 74 90

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
Not Applicable
Sponsor
University Hospital, Basel, Switzerland
Registry
ClinicalTrials.gov
Start date
31 March 2025
Est. completion
1 August 2027

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

Assessment whether intracranial stenting compared to conventional endovascular treatment is beneficial regarding patient's functional status

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: 7 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