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ID04956185

Prospective Observational Study Collecting Data from Patients Admitted to the Stroke Unit for Research and Quality Monitoring

Led by University Hospital, Ghent · Updated on 2025-01-15

5000

Participants Needed

1

Research Sites

509 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are creating a database to collect information from patients admitted to the Stroke unit or other hospital wards with cerebrovascular disease at University Hospital Ghent. This prospective observational study aims to gather data for future research and to monitor important quality indicators in stroke care. All patients included have explicitly given informed consent for their data to be collected. The data collected are part of standard clinical care and include demographic details, medical history, neurological evaluations, results of acute stroke therapies, course of hospitalization including complications and treatments, stroke investigations, and therapy at discharge. No extra tests or procedures will be performed beyond routine care. Follow-up includes assessment of the modified Rankin Score during outpatient visits. Participants will have their clinical data recorded from admission until up to 12 months follow-up. Researchers will monitor outcomes such as stroke characteristics, timing of treatment, therapies received, complications, stroke cause, mortality, and disability. This data collection enables retrospective observational studies and quality tracking without requiring additional patient procedures.

CONDITIONS

Official Title

Data Collection of Patients Admitted to the Stroke Unit

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients admitted to the Stroke unit with a cerebrovascular disease
  • Patients admitted to the regular neurological ward or any other department in the University Hospital Ghent with a cerebrovascular disease who are actively followed by the department of Neurology during hospitalisation
  • Patients who have given their explicit informed consent for data collection
Not Eligible

You will not qualify if you...

  • Patients who have not given informed consent for data collection
  • Patients who are not able to give informed consent and whose legal representative has not given informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Department of Neurology - Ghent University Hospital

Ghent, Flanders, Belgium, 9000

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Research Team

V

Veerle De Herdt, MD PhD

D

Dimitri Hemelsoet, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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