Last reviewed · How we verify

NCT05803759: TEA-CART

The Effects of Allicor on Patients After Coronary Arteria Revascularization Treatment

Status unknown Phase 4 Last updated 19 April 2023
What this trial tests

Phase 4 trial testing Allicor in Myocardial Ischemia in 200 participants. Status unknown.

Timeline
10 April 2023
Primary endpoint
31 March 2024
31 March 2025

Quick facts

Lead sponsorInstitute for Atherosclerosis Research, Russia
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment200
Start date10 April 2023
Primary completion31 March 2024
Estimated completion31 March 2025
Sites1 location across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Institute for Atherosclerosis Research, Russia

Who can join

Adults 40 to 75, any sex, with Myocardial Ischemia or Coronary Artery Bypass Grafting. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Coronary revascularization interventions such as coronary artery bypass graft (CABG) and percutaneous coronary intervention (PCI) are the standard of surgical treatment of patients with myocardial ischemia. However, up to 30% of patients experience complications of varying degrees within 12 months after the revascularization, or need for second intervention. Thus, it is necessary to search for additional approaches to the postoperative treatment of patients in order to improve the long-term results of revascularization treatment. Substances of natural origin with an anti-atherosclerotic effect have a good potential. These substances, as dietary supplements, can be taken by patients for a long time in conjunction with other prescribed medicines and treatments. Another valuable direction of investigations is the search for predictors of long-term cardiovascular complications after revascularization, which can be markers of inflammation and heteroplasmy levels of the patient's mitochondrial genome. The purpose of this study is to determine whether the intake of dietary supplement Allicor at a daily dose of 300 mg affects the frequency of long-term postoperative cardiovascular complications and re-intervention in patients after revascularization operations on the coronary arteries. The second goal is assessing the relationship between the grade monocytes inflammatory response and the level of heteroplasmy of the mitochondrial genome of blood leukocytes with the frequency of cardiovascular complications and re-interventions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Allicor

Trials testing the same drug.

Other recruiting trials for Myocardial Ischemia

Currently open trials in the same condition.

Other Institute for Atherosclerosis Research, Russia 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/NCT05803759.

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