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New Clot-Busting device could save stroke patients

NCT ID NCT07174505

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study tests a new device called the CONDA stent retriever, which is used to remove blood clots from the brain in people having a stroke. About 50 patients will be treated within 24 hours of their symptoms starting. The goal is to see if the device is safe and works well at restoring blood flow.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
CONDA stent retriever (a device to remove blood clots from brain arteries)
What this could lead to
If successful, this could provide a new, safe option for quickly restoring blood flow in stroke patients, potentially reducing disability.
What could go wrong
This is an early, small study with only 50 participants, so results may not apply to everyone. There is a risk of bleeding in the brain from the procedure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2025

An estimate. Start dates often move.

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Age 18 to 85 years. 2. Informed consent was obtained from subject or acceptable subject surrogate (e.g., next of kin, or legal representative). 3. New focal disabling neurologic deficit consistent with acute cerebral ischemia. 4. Baseline NIHSS obtained prior to procedure ≥ 6 points and ≤ 25 points. 5. Pre-ictal mRS score of 0, 1 or 2. 6. Treatable within 24 hours of stroke symptom onset. 7. If indicated, thrombolytic therapy shall be initiated following recommendations established by the AHA/ASA and/or ESO Guidelines. Subjects eligible for IV thrombolysis should receive it without delay. 8. Extended Thrombolysis in Cerebral Infarction (eTICI) Score 0 - 1, confirmed by angiography or CTA/MRA of the: 1. Intracranial internal carotid artery (ICA) 2. Middle cerebral artery - M1 segment 3. Middle cerebral artery - M2 proximal or dominant segments 9. Imaging criteria: * Alberta Stroke Program Early CT Score (ASPECTS) 6 to 10 on baseline CT or DWI-MRI. * If automated assessment, core volume of ≤50 cc on CTP/ DWI-MRI. Exclusion Criteria: The following exclusion criteria will be assessed pre-operatively: 1. Rapid neurological improvement prior to enrollment suggesting resolution of stroke. 2. Subject was diagnosed with a stroke in the last 6 months. 3. Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories. 4. Clinical presentation suggests subarachnoid hemorrhage. 5. Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with antivitamin K, with INR \>3.0. 6. Known baseline glucose of \<50 mg/dL or \>400 mg/dL. 7. Severe, sustained uncontrolled hypertension refractory to treatment (systolic blood pressure \>185 mmHg or diastolic blood pressure \>110 mmHg). 8. Serious, advanced, or terminal disease with anticipated life expectancy of less than 1 year. 9. Known history of severe sensitivity (more than rash) to contrast medium. 10. Known history of severe sensitivity to nickel, titanium metals or their alloys. 11. Known renal insufficiency with creatinine ≥3 mg/dL or glomerular filtration rate (GFR) \<30 mL/min. 12. Subject requires hemodialysis or peritoneal dialysis. 13. Subject is a current user or has a recent history of cocaine and/or heroin use. 14. Known pregnancy and/or lactating female. 15. Subject is participating in a concurrent study involving an investigational drug or device that would impact the primary endpoint of this study. 16. Subject is unlikely to be available for a 90-day follow-up (e.g., no fixed home address, visitor from overseas, etc.) 17. CT or MRI evidence of hemorrhage (the presence of microbleeds is allowed). 18. CT or MRI evidence of significant mass effect with midline shift. 19. CT or MRI evidence of intracranial tumor (except asymptomatic meningioma of ≤ 2cm in diameter). 20. CT or MR evidence of cerebral vasculitis. 21. Suspicion of aortic dissection, presumed septic embolus, or bacterial endocarditis. 22. History of preexisting stent proximal to or at the occlusion site that may preclude safe deployment or recovery of the stent retriever. The following exclusion criteria will be assessed intra-operatively: 23. eTICI score improvement to greater than eTICI 1 after initial screening and prior to intervention. 24. Initially treated with a different thrombectomy device during the current study procedure. 25. Vessel tortuosity too difficult to allow endovascular access of the intracranial internal carotid artery (ICA) per investigator judgement. Indicators of vessel tortuosity include but are not limited to the presence of carotid loops and type 3 aortic arches. 26. Evidence of tandem lesions, including complete occlusion, high-grade stenosis or arterial dissection in the extracranial or intracranial internal carotid artery (ICA), requiring treatment or preventing access to thrombus. 27. Underlying intracranial atherosclerotic disease (ICAD) lesions responsible for the target occlusion. 28. Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation). 29. Inability to gain arterial access.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites in 2 countries. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Semmelweis University Hospital

    NOT_YET_RECRUITING

    Budapest, 1145, Hungary

  • Vall d'Hebron University Hospital

    RECRUITING

    Barcelona, 08035, Spain

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