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NCT07412249: RICSICAS

Remote Ischemic Conditioning Plus Stenting for Symptomatic Carotid Artery Stenosis

Recruiting now NA Last updated 3 April 2026
What this trial tests

NA trial testing Remote ischemic conditioning in Carotid Stenosis in 300 participants. Currently enrolling.

Timeline
4 March 2026
Primary endpoint
30 November 2027
30 November 2027

Quick facts

Lead sponsorGeneral Hospital of Shenyang Military Region
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment300
Start date4 March 2026
Primary completion30 November 2027
Estimated completion30 November 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

General Hospital of Shenyang Military Region

Who can join

40 and older, any sex, with Carotid Stenosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Remote ischemic conditioning (RIC) has emerged as a promising non-invasive strategy to protect the brain, with evidence suggesting its benefit in patients with carotid artery stenting (CAS). However, the long-term benefit and safety of chronic RIC in this population remain unknown. This trial aims to evaluate whether chronic RIC reduces the incidence of major vascular events and improves clinical outcomes in high-risk patients with carotid artery stenosis who received CAS.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Remote ischemic conditioning

Trials testing the same drug.

Other recruiting trials for Carotid Stenosis

Currently open trials in the same condition.

Other General Hospital of Shenyang Military Region trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07412249.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing