Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
500 participants
OBSERVATIONAL
2023-02-21
2024-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
BIC: Evaluation of the Current Care Processes for Stroke Care in Flemish Hospitals
NCT05218135
Effect of Remote Ischemic Conditioning on Vascular Health in Stroke Patients
NCT03635177
Quality Assessment in Acute Stroke Care
NCT00574262
The Care of Stroke in Ziekenhuis Oost-Limburg
NCT03355690
Registry of Acute Ischemic Stroke With Large- or Medium-vessel Occlusion
NCT05779215
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
Completion of questionnaire
Questionnaire
Completion of the patient reported experience measurements (PREMs) questionnaire
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Questionnaire
Completion of the patient reported experience measurements (PREMs) questionnaire
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* ischemic stroke
* stayed at least one day at the stroke unit
Exclusion Criteria
* not able to answer question orally
* are not proficient in the dutch language
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
KU Leuven
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Kris Vanhaecht
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
KU Leuven
Leuven, Flemish Brabant, Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BIC4STROKEPREMS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.