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Study identifier: NCT06931535 Synced from ClinicalTrials.gov · July 28, 2026
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Remote Ischemic Conditioning for Acute Moderate Posterior Ischemic Stroke

Condition: Ischemic Stroke  ·  Sponsor: General Hospital of Shenyang Military Region

PhaseNA
Planned participants960
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A substantial body of basic and clinical research has demonstrated the protective effects of remote ischemic conditioning (RIC) in ischemic stroke. While these clinical studies support the safety of RIC, the neuroprotective benefits of RIC in acute ischemic stroke (AIS) patients lack robust evidence due to small sample sizes, heterogeneous RIC protocols, and variability in the severity of neurological deficits among study populations. Our recent multicenter randomized clinical trial, the RICAMIS study, investigated the efficacy of RIC in patients with acute moderate ischemic stroke. The results showed that RIC administered within 48 hours of onset significantly improved 90-day neurological outcomes in patients with moderate stroke severity. It is well established that anterior circulation stroke (ACS) and posterior circulation stroke (PCS) differ in multiple aspects, including anatomical structure, collateral circulation, blood supply, clinical manifestations, prognosis, ischemic tolerance time, and treatment response. For instance, compared to the anterior circulation, the posterior circulation has poorer collateral circulation, a higher proportion of stroke etiologies attributed to atherosclerosis, and longer ischemic tolerance time. Consequently, intravenous thrombolysis and endovascular therapy may offer a more extended therapeutic time window for PCS patients. A prespecified subgroup analysis of the RICAMIS study revealed that patients with PCS derived greater benefit fr…

This description comes directly from the study's public registry record.

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Locations (1)

Department of Neurology, General Hospital of Northern Theater CommandShenyang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06931535