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NCT06279663: NSTE-ACSMT

Management Tactics for Patients High Risk With Acute Coronary Syndrome Without ST Segment Elevation and Multivessel Coronary Artery Disease

Recruiting now NA Last updated 13 March 2024
What this trial tests

NA trial testing Revascularization in Coronary Syndrome, Acute, Non-ST Elevation, High Risk Patients in 460 participants. Currently enrolling.

Timeline
29 February 2024
Primary endpoint
31 December 2028
31 December 2029

Quick facts

Lead sponsorFederal State Budgetary Institution National Medical Research Center named after academician E.N. Me
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment460
Start date29 February 2024
Primary completion31 December 2028
Estimated completion31 December 2029
Sites2 locations across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Federal State Budgetary Institution National Medical Research Center named after academician E.N. Me

Who can join

18 and older, any sex, with Coronary Syndrome, Acute, Non-ST Elevation, High Risk Patients. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study will include patients with acute coronary syndrome without ST segment elevation and multivessel CA lesion, who are subject to surgical treatment according to KG data (Syntax Score 23 - 32 points with significant damage to the anterior descending artery and/or trunk of the left coronary artery). The patient should be suitable for both CABG and PCI (confirmed by an X-ray surgeon and a cardiac surgeon). An X-ray surgeon and a cardiac surgeon, within the framework of planning the volume of revascularization, strives for the fullest feasible volume. Complete myocardial revascularization (that is, the desire for the absence of hemodynamically significant coronary arteries after revascularization, with a diameter of \> 2.5 mm, that is, residual coronary artery stenosis of no more than 60%). Thus, patients will be randomized into groups in a ratio of 1:1. Each group will need to include 230 patients (a total of 460). In the main group, revascularization will be performed by PCI, in the control group by CABG.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Revascularization

Trials testing the same drug.

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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/NCT06279663.

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