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Funded Projects › H2020

PROOF · Penumbral Rescue by Normobaric O=O Administration in Patients With Ischaemic Stroke and Target Mismatch ProFile: A Phase II Proof-of-Concept Trial

H2020Status: CLOSED1 January 201730 June 2023EU funding €5,246,832Call H2020-SC1-2016-2017

Ischemic stroke (IS), caused by occlusion of arteries that supply blood to the brain, remains a leading cause of mortality and morbidity in the world. Disruption of blood and oxygen supply to the brain leads to neuronal death in the ischemic core within minutes. The hypoperfused tissue surrounding the ischemic core, the penumbra, is at high risk for infarction over time but still salvageable. Neuroprotective “bridging”, sustaining the penumbra until reperfusion, may widen the therapeutic window, make recanalization treatments accessible to more patients and improve overall IS outcomes.As ischemic cell death is primarily mediated by hypoxia, increasing oxygen supply to the penumbra seems THE logical approach. In animal models of IS, normobaric hyperoxygenation (NBHO) significantly increased penumbral oxygen pressure and attenuated brain injury when initiated early after onset of ischaemia and vessel occlusion was transient (35 to 50% infarct volume reduction).The PROOF project now seeks to demonstrate that NBHO (high-flow 100% oxygen at >45 L/min via a non-rebreather mask, or FiO2=1.0 for intubation/ventilation) reduces infarct growth from baseline to 24 hours compared to standard treatment if administered ≤3 hours after onset of anterior circulation IS, in patients with proximal vessel occlusion and salvageable tissue at risk. The study is multi-center, adaptive phase-IIb, randomized, open-label with blinded-endpoint (PROBE design).The primary efficacy criterion will be infarct growth from baseline to 24 hours. Secondary endpoints will be NIHSS 24h, categorical shift in the pre-stroke modified Rankin Score, QoL and cognition at day 90.Potential surrogate biomarkers, health economics and societal impacts will be assessed.If NBHO proves its neuroprotective potential in this selected population, phase-III trials in all IS patients may be undertaken. Considering its low costs and ease of use, NBHO may impact stroke care worldwide.

Consortium · 16 organisations

coordinator

EBERHARD KARLS UNIVERSITAET TUEBINGEN

DE · €1,539,209

participant

ECRIN EUROPEAN CLINICAL RESEARCH INFRASTRUCTURE NETWORK

FR · €368,008

participant

FAKULTNI NEMOCNICE U SV ANNY V BRNE

CZ · €76,692

participant

HUS-YHTYMA

FI · €117,901

thirdParty

LUXEMBOURG INSTITUTE OF HEALTH

LU

thirdParty

Masarykova univerzita

CZ

thirdParty

UNIVERSITAETSKLINIKUM TUEBINGEN

DE

participant

STROKE ALLIANCE FOR EUROPE

BE · €66,625

participant

CENTRE HOSPITALIER UNIVERSITAIRE VAUDOIS

CH · €26,225

participant

GROUPE HOSPITALIER UNIVERSITAIRE PARIS PSYCHIATRIE ET NEUROSCIENCES

FR · €103,347

participant

VASTRA GOTALANDSREGIONEN

SE · €3,949

participant

UNIVERSITATSKLINIKUM HEIDELBERG

DE · €1,270,874

participant

EPPDATA GMBH

DE · €737,875

participant

KATHOLIEKE UNIVERSITEIT LEUVEN

BE · €159,625

participant

FUNDACIO HOSPITAL UNIVERSITARI VALL D'HEBRON - INSTITUT DE RECERCA

ES · €776,503

thirdParty

KKS-NETZWERK EV -NETZWERK DER KOORDINIERUNGSZENTREN FUR KLINISCHE STUDIEN

DE

Research fields

View the official record on CORDIS →

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