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CLEAR-FDR Stroke Trial

The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. The primary outcome variable is the proportion of patients who experience sICH as defined in the NINDS stroke trial. Secondary outcomes include: the presence of any ICH and the proportion of patients who develop parenchymal hemorrhage types 1 (PH-1) and 2 (PH-2); and, 90 day outcomes as measured by the modified Rankin score.

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CLEAR-FDR Stroke Trial | clear-fdr.org Reviews

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The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. The primary outcome variable is the proportion of patients who experience sICH as defined in the NINDS stroke trial. Secondary outcomes include: the presence of any ICH and the proportion of patients who develop parenchymal hemorrhage types 1 (PH-1) and 2 (PH-2); and, 90 day outcomes as measured by the modified Rankin score.

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CLEAR-FDR Stroke Trial | clear-fdr.org Reviews

https://clear-fdr.org

The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. The primary outcome variable is the proportion of patients who experience sICH as defined in the NINDS stroke trial. Secondary outcomes include: the presence of any ICH and the proportion of patients who develop parenchymal hemorrhage types 1 (PH-1) and 2 (PH-2); and, 90 day outcomes as measured by the modified Rankin score.

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clear-fdr.org

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Publications :: CLEAR-FDR Stroke Trial

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The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. CLEAR manuscript April 2008. CLEAR-ER manuscript September 2013. Overview and rationale for the CLEAR stroke trials.

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CLEAR-FDR Stroke Trial

http://clear-fdr.org/index.html

The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. The primary outcome variable is the proportion of patients who experience sICH as defined in the NINDS stroke trial. Secondary outcomes include: the presence of any ICH and the proportion of patients who develop parenchymal hemorrhage types 1 (PH-1) and 2 (PH-2); and, 90 day outcomes as measured by the modified Rankin score.

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CLEAR-FDR Stroke Trial

The CLEAR-FDR Stroke Trial. The Combined Approach to Lysis Utilizing Eptifibatide and rt-PA in Acute Ischemic Stroke – Full Dose Regimen. Opeolu M. Adeoye MD. The primary outcome variable is the proportion of patients who experience sICH as defined in the NINDS stroke trial. Secondary outcomes include: the presence of any ICH and the proportion of patients who develop parenchymal hemorrhage types 1 (PH-1) and 2 (PH-2); and, 90 day outcomes as measured by the modified Rankin score.

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