Schlaganfallkonsortium Rhein-Neckar (Stroke Consortium Rhine-Neckar)
FAST
1 other identifier
observational
12,000
1 country
1
Brief Summary
FAST is an investigator-initiated multicenter study embedded in a German multistate acute stroke network. The main objectives of the FAST study are to improve outcomes and quality of care for stroke patients, to quantify the number of patients in need of thrombectomy within an integrated stroke network, to study the best way of delivering and performing thrombectomy and to investigate the best model of pre-hospital selection and referral for stroke patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 16, 2017
CompletedFirst Posted
Study publicly available on registry
May 17, 2017
CompletedStudy Start
First participant enrolled
October 26, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2024
CompletedNovember 29, 2023
November 1, 2023
6.1 years
May 16, 2017
November 28, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Functional outcome
Functional outcome according to the modified Rankin Scale (mRS)
3 months after intervention
Secondary Outcomes (2)
Number of patients receiving acute recanalisation therapies of all referrals
24 h after stroke onset
Referral rates
Stroke onset to discharge from acute hospital; through study completion, an average of 2 years
Study Arms (3)
Primary CSC (Comprehensive Stroke center) admission
Patients with primary admission to endovascular-ready hospital (comprehensive stroke center)
Primary non-CSC (non-Comprehensive Stroke Center) SU (Stroke Unit) admission
Patients with primary admission to non-endovascular-ready hospital with (regional/local) stroke unit
Non-acute stroke hospital admission
Patients with primary admission to non-acute stroke-ready hospital
Interventions
Observational study without study related intervention
Eligibility Criteria
Acute stroke patients admitted to one of the hospitals of the Stroke Consortium Rhein-Neckar (FAST)
You may qualify if:
- years or older
- Patients with ischemic stroke who are admitted to one of the hospitals of the Stroke Consortium Rhein-Neckar (FAST)
- informed consent
You may not qualify if:
- no informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital Heidelberglead
- Dietmar Hopp Stiftungcollaborator
Study Sites (1)
Heidelberg University Hospital
Heidelberg, 69120, Germany
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wolfgang Wick, Prof. Dr.
University Hospital Heidelberg
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chairman of the Neurologic Clinic
Study Record Dates
First Submitted
May 16, 2017
First Posted
May 17, 2017
Study Start
October 26, 2017
Primary Completion
December 1, 2023
Study Completion
March 1, 2024
Last Updated
November 29, 2023
Record last verified: 2023-11