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Reasons for Prehospital Delay in Patients With Acute Ischemic Stroke

University Hospital Basel logo

University Hospital Basel

Status

Completed

Conditions

Acute Ischemic Stroke

Treatments

Other: No Intervention Foreseen

Study type

Observational

Funder types

Other

Identifiers

NCT02798770
UBE-15/64

Details and patient eligibility

About

Ischemic stroke is the leading cause of acquired disability among adults, and one of the main causes of death. In Switzerland, the approved time window for stroke treatment with intravenous thrombolysis after symptom onset is 4.5 h. Even within the 4.5 h time-window, however, the benefit of treatment strongly decreases as time passes.

Moreover, only around 10% patients receive thrombolytic treatment, since patients with stroke arrive too late to the hospital (prehospital delay). Despite efforts to educate the community on the symptom of stroke, prehospital delay did not decrease over time, and the reasons remain incompletely understood. Prehospital delay reduces the proportion of patients with ischemic stroke treated with thrombolysis, and reduces the odds of favorable outcome among the minority treated with thrombolysis.

This prospective cohort study aims at understanding the causes of prehospital delay among patients with acute ischemic stroke. Trained study-nurses will interview, at the bedside, patients and proxies along a standardized questionnaire on prehospital delay. Avoiding modificables causes of prehospital delay may increase the thrombolysis rate and improve outcomes after stroke.

Enrollment

337 patients

Sex

All

Ages

17+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with an acute ischemic stroke hospitalized in the Stroke Center of the University Hospital Basel.

Exclusion criteria

  • Patient not able to answer the in-person, bedside questionnaire asked by a trained study Nurse.
  • Patient not willing to participate to the study

Trial design

337 participants in 1 patient group

Stroke Center Basel
Treatment:
Other: No Intervention Foreseen

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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