Clinical trial Recruiting at 1 site Observational Ages 18 and up

Reperfusion injury after mechanical thrombectomy for stroke

Official title: Hemodynamic Changes and Reperfusion Injury After Endovascular Stroke Treatment: Prospective Multicenter DYNASTROKE STUDY

Run by Medical University of Graz · NCT05273216 · Data updated 2026-11-12

This project tests whether bedside transcranial Duplex sonography together with MRI and blood markers can find patients at higher risk of brain bleeding or swelling after mechanical thrombectomy for large-vessel ischemic stroke.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment600 (estimated)
SponsorMedical University of Graz
Academic / other
Locations3 sites (Graz, Styria and 2 other locations)
StatusRecruiting
StartedOctober 1, 2021
Main results expectedJuly 2026
Study endsJuly 2026
Registry record updatedJune 13, 2025
Trial IDNCT05273216 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults (≥18 years) with anterior-circulation large-vessel occlusion who receive mechanical thrombectomy at one of the participating centers.

Probably not a fit

Patients with basilar artery occlusion, those treated outside the participating hospitals, or individuals under 18 are not eligible and are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, longitudinal multicenter study enrolling adults with anterior-circulation large vessel occlusion treated with mechanical thrombectomy at three Austrian stroke centers. Participants will undergo serial bedside transcranial Duplex sonography to detect increased flow velocity in the recanalized middle cerebral artery, perfusion MRI to confirm cerebral hyperperfusion, and blood sampling for biomarkers of blood-brain-barrier and neuroaxonal injury. The study will correlate these hemodynamic and biomarker findings with short-term outcomes including intracranial hemorrhage and vasogenic edema. The goal is to characterize reperfusion-related hemodynamic changes and identify bedside screening methods that predict post-thrombectomy complications.

Why it matters

Potential benefit: If successful, the approach could enable early identification of patients at high risk of post-thrombectomy bleeding or edema so clinicians can intensify monitoring or adjust therapies to reduce complications.

How similar studies have gone: Small pilot studies have suggested bedside TCD can detect hyperperfusion associated with later hemorrhage, but multicenter prospective confirmation is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* stroke due to large vessel occlusion of the anterior cerebral circulation (internal carotid artery, middle cerebral artery) receiving mechanical thrombectomy.

Exclusion Criteria:

* basilar artery occlusion
* age below 18 years

Where it's running

  • Medical Univerity of Graz, Department of Neurology
    Graz, Styria, Austria
    Recruiting
  • Medical University of Innsbruck, Department of Neurology
    Innsbruck, Tyrol, Austria
    Not yet recruiting
  • Paracelsus Medical University, Department of Neurology
    Salzburg, Austria
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals

    This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.

    Recruiting at 2 sites Hospital Universitari Vall d'Hebron Research Institute · Leuven and 6 other locations · NCT07924371

  • Remote ischemic conditioning for post-stroke insomnia

    A 136-person, randomized study will test whether a non-invasive arm-cuff procedure done twice daily for 90 days can improve sleep after a first ischemic stroke in adults 18–80.

    Recruiting Sichuan Academy of Medical Sciences · Chengdu, Sichuan · NCT07874594

  • Ear-based nerve stimulation to help sleep after a stroke

    A device that delivers vagal nerve stimulation through the ear is tested to see if it helps stroke patients in rehab sleep better.

    Recruiting Casa Colina Hospital and Centers for Healthcare · Pomona, California · NCT07858656

  • Theta Burst Stimulation to Help Stroke Recovery (Upper and Lower Limbs)

    This trial tests whether applying theta burst stimulation to the motor cortex, in combination with standard rehabilitation, helps people over 45 who recently had a first ischemic stroke recover arm and leg movement.

    Recruiting Ankara Etlik City Hospital · Ankara, Yenimahalle · NCT07834333

  • Preventing another ischemic stroke with a smart bracelet and app

    This study tests whether a digital prevention program using a wearable and a mobile app can help people who recently had an ischemic stroke reduce the chance of another stroke and improve risk-factor control.

    Recruiting Affiliated Hospital of Nantong University · Nantong, Jiangsu · NCT07825311

  • Photon-counting CT to check intracranial stents

    This study tests whether ultra-high-resolution photon-counting CT can reliably visualize intracranial stents and detect in-stent restenosis during follow-up of patients with prior stents.

    Recruiting Chinese PLA General Hospital · Beijing, Beijing Municipality · NCT07769814

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.