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Checking for a Treatment Target in Acute Brain Bleeding

Tests a dye-based scan of brain blood vessels in adults with sudden brain bleeding.

Plain-language title generated from the registry record
Registry title: Detection of an Endovascular Treatment Target in Patients With an Acute, Spontaneous Intracerebral Hemorrhage

Key facts

Where
Basel, SwitzerlandSee the site

Where in Switzerland

  • Department of Neuroradiology, University Hospital BaselBasel, SwitzerlandTaking people

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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT05504941
Record updated
11 April 2025
Original description
This study is to determine if a treatment target for a potential endovascular therapy exists in patients with an acute, spontaneous (non-traumatic) ICH.Read full original descriptionShow less

Detection of an Endovascular Treatment Target in Patients With an Acute, Spontaneous Intracerebral Hemorrhage - an EXPLOrative Pilot Study (HemEXPLO)

This study is to determine if a treatment target for a potential endovascular therapy exists in patients with an acute, spontaneous (non-traumatic) ICH.

Inclusion: Diagnosis of an acute spontaneous ICH based on non-contrast CT; Time from symptom onset to anticipated start of cerebral DSA of under 3 hours; Agreement of the treating physician to perform DSA; Informed consent documented by signature or fulfilling the criteria for emergency consent procedures (deferral of consent).

Exclusion: Any time critical surgical or minimal invasive intervention is planned; High probability that the etiology of the bleeding is a ruptured aneurysm, an arteriovenous malformation or an amyloid angiopathy as judged by the treating physician; Known severe kidney insufficiency (Glomerular filtration rate < 30 ml/min); Evidence of an ongoing pregnancy, a negative pregnancy test is mandatory in all persons of childbearing potential; Contraindications against the use of iodine contrast media.

ClinicalTrials.gov NCT05504941