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STOP-stroke: STroke Outcome Prediction in the Acute Treatment Setting - a Prospective, Single-center, Observational Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The STOP-stroke project aims at improving prediction of outcome early after stroke. In order to achieve this, we need to understand reasons (important variables) for prediction in a real clinical prognostication process. We aim to: 1. Test the predictive performance of stroke neurologists for outcome prediction (NIHSS at 24 hours and 3 months and mRS at 3 months after stroke onset) prospectively and in a real clinical setting, and to explore the most important baseline variables in their prognostication process. 2. Test the prediction performance of our DL models when being provided with structured clinical and/or imaging information from the same patients as the neurologists; and to discover most relevant features of the input data. 3. Use the information gained from our experiments for improving our DL algorithm. This will include an error analysis on the missclassifications of models and neurologists to understand the pitfalls of both approaches. We anticipate to develop a robust, reliable and clinically feasible application ready for testing in a prospective, observational trial.

Eligibility
Participation Requirements
Sex: All
View:

• Patients from up to 18 years years of age without any upper age limit.

• Patients with clinical suspicion of acute ischemic stroke (acute onset focal neurological deficit) at the discretion of the paramedic or treating physician within 24 hours of symptom onset including wake-up situation and unclear symptom onset planned for clinically indicated neuroimaging.

• Patients with externally performed neuroimaging before admission or referral to the USZ will be included from the time point N2 on if no refusal of use of data is documented.

Locations
Other Locations
Switzerland
University Hospital Zurich, Department of Neurology
RECRUITING
Zurich
Contact Information
Primary
Laura Philine Westphal, MD
lauraphiline.westphal@usz.ch
0041432537590
Backup
Susanne Wegener, MD
susanne.wegener@usz.ch
Time Frame
Start Date: 2024-10-29
Estimated Completion Date: 2027-07-30
Participants
Target number of participants: 250
Related Therapeutic Areas
Sponsors
Leads: University of Zurich

This content was sourced from clinicaltrials.gov