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Search / Trial NCT06037200

Urin-based Point-of-Care Testing for Direct Oral Anticoagulants in Stroke Patients

Launched by UNIVERSITY OF GIESSEN · Sep 13, 2023

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Oral Anticoagulation Direct Oral Anticoagulants Point Of Care Test

ClinConnect Summary

This clinical trial is studying a new urine test designed to quickly identify if stroke patients have taken certain blood-thinning medications known as direct oral anticoagulants (DOACs). The main goals are to see if this urine test can effectively detect these medications, whether it provides faster results compared to traditional blood tests, and if it can be easily used in emergency settings for stroke care. The trial is currently looking for participants aged 18 and older who have been diagnosed with either ischemic (caused by a blockage) or hemorrhagic (caused by bleeding) stroke and are being treated at the University Hospital Giessen.

If you or a family member are considering participating, you'll need to have been admitted for a stroke and may need to meet specific criteria related to medication intake. Participants can expect to undergo the urine test as part of their care, and the study will help researchers understand the benefits of using this new testing method in urgent situations. It's important to note that some patients may not be eligible if they have certain medical conditions or if they require specific treatments.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patient age ≥18 years at the time of admission
  • Clinical diagnosis of ischemic or hemorrhagic stroke.
  • Treatmet at our certified stroke-unit, University Hospital Giessen.
  • Phase 1 only: Confirmed intake of a direct oral anticoagulant (DOAC) for at least 48 hours (test group) or no intake of a DOAC (control group for specificity determination)
  • Phase II only, anamnestic intake of DOAC or no information about OAC-intake.
  • Phase II only, presentation with 4.5 hours after onset.
  • Exclusion Criteria (only Phase II):
  • Contraindications for intravenous thrombolysis other than intake of DOAC
  • large vessel occlusion with indication for immediate endovascular thrombectomy
  • chronic renal insufficiency with need for hemodialysis

About University Of Giessen

The University of Giessen, a prominent research institution in Germany, is dedicated to advancing medical science through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, the university leverages its expertise in various fields, including medicine, pharmacology, and public health, to conduct rigorous studies aimed at improving patient outcomes. Committed to maintaining the highest ethical standards and regulatory compliance, the University of Giessen fosters a research environment that encourages scientific inquiry and the translation of findings into clinical practice, ultimately contributing to the advancement of healthcare and therapeutic strategies.

Locations

Gießen, Hesse, Germany

Patients applied

0 patients applied

Trial Officials

Stefan Gerner, MD

Principal Investigator

Department of Neurology, University Hospital Giessen/Germany

Thorsten Doeppner, MD

Study Chair

Department of Neurology, University Hospital Giessen/Germany

Hagen Huttner, MD, PhD

Study Chair

Department of Neurology, University Hospital Giessen/Germany

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported