Last reviewed · How we verify
NCT06279663: NSTE-ACSMT
Management Tactics for Patients High Risk With Acute Coronary Syndrome Without ST Segment Elevation and Multivessel Coronary Artery Disease
NA trial testing Revascularization in Coronary Syndrome, Acute, Non-ST Elevation, High Risk Patients in 460 participants. Currently enrolling.
31 December 2028
Quick facts
| Lead sponsor | Federal State Budgetary Institution National Medical Research Center named after academician E.N. Me |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 460 |
| Start date | 29 February 2024 |
| Primary completion | 31 December 2028 |
| Estimated completion | 31 December 2029 |
| Sites | 2 locations across Russia |
Drugs / interventions tested
- Revascularization
Conditions studied
- Coronary Syndrome, Acute, Non-ST Elevation, High Risk Patients — all drugs for Coronary Syndrome, Acute, Non-ST Elevation, High Risk Patients →
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.
Verify or expand the search:
- PubMed search for NCT06279663
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06279663 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Federal State Budgetary Institution National Medical Research Center named after academician E.N. Me
- Last refreshed: 13 March 2024
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