Emergency control center-based identification of stroke patients for thrombectomy and improvement of the process of rescue

Not Applicable

• Conditions: I63; Cerebral infarction

• Registration Number: DRKS00022152
• Lead Sponsor: Klinik für Neurologie und Neurophysiologie, Universitätsklinikum Freiburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-10-19
• Study Completion: 2024-02-29
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 396

Inclusion Criteria

Patients, who are older than 18 years and suffered a stroke with large vessel occlusion (LVO), that can be treated within 24 hours after occurrence of the first symptoms.

Exclusion Criteria

Patients with preexisting severe disabilities caused by other diseases (degree 5 of disability according to the modified Rankin-Scale: bedridden, incontinent, needs permanent care), analogue to previous large thrombectomy studies.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary Outcome is the clinical outcome, measured by the modified Rankin-Scale (degress of disability/limitations of activities) 90 days after treatment. Patients will be interviewed by telefone (blinded survey).

Secondary Outcome Measures

Name	Time	Method
Secondary Outcomes are time durations of preclinical and clinical treatment, clinical criteria and outcomes of imaging methods, lenght of the hospital stay, number of hemicraniaectomy and mortality.