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Search / Trial NCT05504941

Detection of an Endovascular Treatment Target in Patients With an Acute, Spontaneous Intracerebral Hemorrhage

Launched by UNIVERSITY HOSPITAL, BASEL, SWITZERLAND · Aug 15, 2022

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Digital Subtraction Angiography (Dsa) Hemorrhagic Stroke Hematoma Expansion Cerebral Dsa

ClinConnect Summary

This clinical trial is looking to find a specific treatment target for patients who have experienced an acute, spontaneous bleeding in the brain, known as an intracerebral hemorrhage (ICH). The goal is to see if a certain type of therapy that is delivered through blood vessels (called endovascular therapy) could be beneficial for these patients. The study is currently recruiting participants aged 65 to 74 who have been diagnosed with ICH and are within three hours of their symptoms starting.

To be eligible for the trial, participants must have a confirmed diagnosis of ICH through a type of brain scan called a CT scan. They also need to have the agreement of their doctor to undergo a special imaging procedure known as digital subtraction angiography (DSA). However, individuals who have certain conditions, such as a high chance that their bleeding is due to specific causes like an aneurysm or who are pregnant, will not be eligible. Participants in the trial can expect to undergo DSA to help determine the best treatment options for their condition, and their safety will be closely monitored throughout the study.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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 Criteria:
  • 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
  • Any time critical surgical or minimal invasive intervention is planned
  • 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
  • Known severe kidney insufficiency (Glomerular filtration rate \< 30 ml/min)

About University Hospital, Basel, Switzerland

The University Hospital Basel, Switzerland, is a leading academic medical center renowned for its commitment to cutting-edge research and innovative patient care. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to advance medical knowledge and therapeutic options across various disciplines. With a collaborative approach that integrates clinical practice and scientific inquiry, the University Hospital Basel fosters an environment conducive to rigorous clinical trials, ensuring the highest standards of safety and efficacy. Its strategic focus on patient-centered research aims to translate scientific discoveries into tangible health solutions, benefiting both local and global communities.

Locations

Basel, , Switzerland

Patients applied

0 patients applied

Trial Officials

Marios-Nikos Psychogios, Prof Dr

Study Director

Department of Neuroradiology, University Hospital Basel

Urs Fischer, Prof Dr

Study Chair

Department of Neurology, University Hospital Basel

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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