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REGistry of Long-term AnTithrombotic TherApy-1

Registry Dedicated to Assess the Risk of Ischemic and Hemorrhagic Complications of Long-term Antithrombotic Therapy in Patients With Chronic Coronary Syndromes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04347200
Acronym
REGATTA-1
Enrollment
2000
Registered
2020-04-15
Start date
2015-01-15
Completion date
2026-01-31
Last updated
2025-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease (CAD) (E.G., Angina, Myocardial Infarction, and Atherosclerotic Heart Disease (ASHD)), Peripheral Artery Disease

Keywords

Coronary Artery Disease, Peripheral Artery Disease

Brief summary

To assess the rates of ischemic and hemorrhagic complications of long-term antithrombotic therapy in patients with chronic coronary syndromes

Detailed description

The register is a Russian prospective single-center observational study of patients who have indications for long-term antithrombotic therapy in connection with chronic coronary syndromes

Interventions

single or dual antiplatelets, triple antithrombotic therapy

Sponsors

National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* coronary artery disease , confirmed by history of myocardial infarction, or revascularization, or definitive evidence of CAD on imaging

Exclusion criteria

* Subjects who are unwilling or unable to provide informed consent. * Acute coronary syndrome within 12 months before inclusion * Severe chronic heart failure (NYHA IV) * Stroke within 6 months before inclusion * Severe liver or muscle disease * Severe kidney disease / renal failure with creatinine \> 3 mg/dl * Conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention -

Design outcomes

Primary

MeasureTime frameDescription
composite of major adverse cardiovascular events (MACE)inclusion up to 5 yearsstroke, myocardial infarction, stent thrombosis \[definite or probable\], or urgent revascularization, cardiac death
composite of any bleeding eventsinclusion up to 5 yearsmajor, clinically relevant nonmajor, minor (BARC, ISTH)

Secondary

MeasureTime frameDescription
Severity of peripheral atherosclerosisinclusionAssessment will be performed with the use of duplex scanning
Mutations in following genesinclusionCYP2C19\*, ABCB1

Countries

Russia

Contacts

Primary ContactAndrey Komarov, PhD
andrkomarov@mail.ru+79161813257

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026