Large Vessel Occlusion Clinical Trial
— RESCUE-ICASOfficial title:
Registry of Emergent Large veSsel oCclUsion duE to IntraCranial AtherosclerosiS
Verified date | March 2024 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The aim of this study is to develop an international multicenter registry of patient data and outcomes for patients undergoing mechanical thrombectomy for emergent large vessel occlusion with residual underlying stenosis following successful revascularization.
Status | Active, not recruiting |
Enrollment | 600 |
Est. completion date | June 14, 2024 |
Est. primary completion date | March 5, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - All patients undergoing mechanical thrombectomy - AND have intracranial stenosis - Patients aged 18-90 years Exclusion Criteria: - None |
Country | Name | City | State |
---|---|---|---|
Germany | Universitätsmedizin Göttingen | Göttingen | |
Italy | Careggi Universtiy Hospital | Florence | |
Portugal | Nova University Lisbon | LIsbon | |
Saudi Arabia | Imam Abdulrahman Alfaisal University | Dammam | |
Switzerland | Universitätsspital Basel | Basel | |
United States | Emory Univeristy Hospital | Atlanta | Georgia |
United States | Massachuestts General Hospital | Boston | Massachusetts |
United States | Medical University of South Carolina | Charleston | South Carolina |
United States | Univeristy of Chicago Medicine | Chicago | Illinois |
United States | Indiana Health Univeristy Hospital | Indianapolis | Indiana |
United States | Univeristy of Iowa Hospital | Iowa City | Iowa |
United States | The University of Tennessee Health Science Center | Memphis | Tennessee |
United States | Univeristy of Miami Health System | Miami | Florida |
United States | Yale New Haven Hospital | New Haven | Connecticut |
United States | Advocate Aurora Health | Oak Lawn | Illinois |
United States | Thomas Jefferson University Hospital | Philadelphia | Pennsylvania |
United States | Brown University | Providence | Rhode Island |
United States | Univeristy of Texas Health Science Center at San Antonio | San Antonio | Texas |
United States | Atrium Health Wake Forest Baptist | Winston-Salem | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina | advocate christ medical center, Brown University, Careggi Hospital, Centro Hospitalar de Lisboa Central, Emory University, HCA Houston Healthcare Kingwood, Imam Abdulrahman Bin Faisal University, Indiana University, Massachusetts General Hospital, Sutter Health, The University of Texas Health Science Center at San Antonio, Thomas Jefferson University, University of Basel, University of Chicago, University of Göttingen, University of Iowa, University of Miami, University of Tennessee, Wake Forest University Health Sciences, Yale University |
United States, Germany, Italy, Portugal, Saudi Arabia, Switzerland,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | modified Rankin score | standard stroke score measuring disability level delivered by physician with level 0-6 with 0 being no symptoms and 6 being death. Outcome measured by the distribution of mRS score. | pre-stroke | |
Primary | modified Rankin score | standard stroke score measuring disability level delivered by physician with level 0-6 with 0 being no symptoms and 6 being death. Outcome measured by the distribution of mRS score. | 7 days | |
Primary | modified Rankin score | standard stroke score measuring disability level delivered by physician with level 0-6 with 0 being no symptoms and 6 being death. Outcome measured by the distribution of mRS score. | admission | |
Primary | modified Rankin score | standard stroke score measuring disability level delivered by physician with level 0-6 with 0 being no symptoms and 6 being death. Outcome measured by the distribution of mRS score. | 3 months | |
Primary | Mortality | Death at 90 days post intervention | 90 day |
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