Clinical trial Recruiting at 1 site Observational Ages 18 and up

Registry of long-term antithrombotic therapy for coronary artery disease

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

Run by National Medical Research Center for Cardiology, Ministry of Health of Russian Federation · NCT04347200 · Data updated 2026-11-12

This study looks at how safe and effective long-term blood-thinning treatments are for people with coronary artery disease, including those who have had heart attacks or heart surgeries.

More Peripheral Artery Disease trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment2000 (estimated)
SponsorNational Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Government
Locations1 site (Moscow)
StatusRecruiting
StartedJanuary 15, 2015
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedMay 1, 2026
Trial IDNCT04347200 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are patients with confirmed coronary artery disease who require long-term antithrombotic therapy.

Probably not a fit

Patients with acute coronary syndrome within the past 12 months or severe comorbid conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the rates of ischemic and hemorrhagic complications associated with long-term antithrombotic therapy in patients suffering from chronic coronary syndromes. Conducted at a single center in Russia, it focuses on individuals with confirmed coronary artery disease, including those with a history of myocardial infarction or revascularization. The study will collect data on the effectiveness and safety of antiplatelet drugs over an extended period.

Why it matters

Potential benefit: If successful, this study could improve the management and safety of antithrombotic therapy in patients with coronary artery disease.

How similar studies have gone: Other studies have shown varying degrees of success with long-term antithrombotic therapy in similar patient populations, but this specific registry approach is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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 -

Where it's running

  • National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
    Moscow, Russia
    Recruiting

Study contacts

  • Principal investigator: Elizaveta Panchenko, PhD — National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
  • Study coordinator: Andrey Komarov, PhD
  • Email: andrkomarov@mail.ru
  • Phone: +79161813257

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.