Trial reportJournal of the American Heart Association2026
Head Down Position Before Endovascular Treatment for Large Vessel Occlusion: Clinical Trial Design.
Trial report in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07172789 (Head dOwn Position Before Endovascular Treatment for Large veSsel Occlusion), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Head dOwn Position Before Endovascular Treatment for Large veSsel Occlusion (HOPES5): a Prospective, Randomized, Open Label, Blinded-end Point, Multi-center Study
Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundHead down position (HDP) shows potential benefits in acute ischemic stroke. Although -20° HDP appears safe, feasible, and potentially beneficial in patients with large artery atherosclerosis without reperfusion therapy, its value before endovascular treatment (EVT) in acute large vessel occlusion (LVO) stroke remains unknown. This trial aims to investigate the efficacy and safety of -20° HDP in patients with acute large vessel occlusion stroke before planned EVT.
methodsThe HOPES5 (Head Down Position Before Endovascular Treatment for Large Vessel Occlusion) trial is a prospective, randomized, open label, blinded-end point, multicenter study. Eligible patients with large vessel occlusion will be randomized 1:1 to -20° HDP or a flat (0°) head position before EVT, alongside standard guideline-based care. Primary outcome is early neurological improvement, defined as ≥4 National Institutes of Health Stroke Scale score reduction within 24 hours post EVT. Safety outcomes are HDP-related adverse events. Based on a prospective cohort, the proportion of early neurological improvement after EVT was ∼31%. A 20% absolute early neurological improvement increase (51%) in the HDP group is assumed. With 2-sided α=0.05, 80% power, 10% follow-up loss, and interim analysis alpha consumption, 210 patients (105 per group) are enrolled. All outcomes will have blinded assessment and will be analyzed on the intention-to-treat basis. The primary analysis will be stratified by age, sex, diabetes, baseline systolic blood pressure, location of index vessel, baseline National Institutes of Health Stroke Scale score, onset to HDP time, onset to thrombectomy time.
conclusionsThe results of HOPES5 will provide initial evidence on the effect of HDP in patients with acute large vessel occlusion stroke before EVT within 24 h of onset. REGISTRATION: URL: https://clinicaltrials.gov/; Unique Identifier: NCT07172789.
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