ACS Registry - A Non-interventional Study to Estimate the Rates of Outcomes in ACS Patients in Moscow

Sponsor
AstraZeneca (Industry)
Overall Status
Completed
CT.gov ID
NCT03654157
Collaborator
(none)
1,576
27
42.8
58.4
1.4

Study Details

Study Description

Brief Summary

Cardiovascular diseases (CVD) are currently the leading cause of death in industrialized countries and are expected to become the leading cause of death in emerging countries by 20201. According to the official Russian statistics, in 2015, CVD was the cause in 34% of deaths in Russia2.

Acute Coronary Syndrome (ACS) is the most prevalent manifestation of CVD and is associated with high mortality and morbidity. No other life-threatening disease is as prevalent or expensive to society3. In 2014 in Russian Federation 46 250 people died from acute myocardial infarction (MI) and 17 605 people died from recurrent MI4.

ACS is a clinical syndrome characterized by unstable angina (UA), non-ST-segment elevation myocardial infarction (NSTEMI) and ST-segment elevation myocardial infarction (STEMI). The most common cause of ACS is reduced myocardial perfusion that results from coronary artery narrowing caused by the formation of partially or totally occlusive thrombi in response to rupture of atherosclerotic plaques on the vessel wall5-7.

In Russian Federation ACS management after ACS is provided in out-patient settings by doctors of different specialties (cardiologists and general practitioners (GPs)). However, the management of ACS in out-patient settings in some regions in Russian Federation is frequently suboptimal. Moscow city significantly differs from other parts of Russia from ACS management at hospital stage (up to 90% of PCI managed ST elevation myocardial infarction (MI) patients, no thrombolysis, short first medical contact to balloon time etc.) but it is unclear if management of post MI patients in Moscow out-patient settings is also optimal. In-hospital mortality in MI patients decreased last years but there is no data on clinical outcomes during 12 months after MI in Moscow.

This study will provide the epidemiological data about rates of major adverse cardiovascular and cerebrovascular events (MACCE) (MI, stroke, cardiovascular death) within 12 months after MI in real clinical practice in Moscow and describe DAPT at out-patient setting. The information received in this study will help to optimize management of Russian patients with ACS. The data will be used in discussion with payers

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1576 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    A Non-interventional Study to Estimate the Rates of Outcomes in ACS Patients in Moscow
    Actual Study Start Date :
    Mar 25, 2018
    Actual Primary Completion Date :
    Oct 19, 2021
    Actual Study Completion Date :
    Oct 19, 2021

    Outcome Measures

    Primary Outcome Measures

    1. the cumulative incidence of Major Adverse Cardiovascular and Cerebrovascular Events (MACСE) [1 year]

      The primary objective of this study is to describe the cumulative incidence of Major Adverse Cardiovascular and Cerebrovascular Events (MACСE) [MI, stroke, and cardiovascular death] observed over 1 year after index MI in all patients enrolled in the study.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    The subject population that will be observed in this prospective study must meet the following criteria:

    1. Patients survivors who visited outpatient setting after discharge from hospital due to MI (STEMI or NSTEMI) within 1 month after discharge from hospital;

    2. Obtained written informed consent for participation in this study.

    3. Age of 18 year or older.

    Exclusion Criteria:
    1. Current participation in a clinical study.

    2. Unknown type of MI

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Research Site Moscow Moscow/Russia Russian Federation 105264
    2 Research Site Moscow Moscow/Russia Russian Federation 107023
    3 Research Site Moscow Moscow/Russia Russian Federation 107564
    4 Research Site Moscow Moscow/Russia Russian Federation 109431
    5 Research Site Moscow Moscow/Russia Russian Federation 109451
    6 Research Site Moscow Moscow/Russia Russian Federation 109548
    7 Research Site Moscow Moscow/Russia Russian Federation 111401
    8 Research Site Moscow Moscow/Russia Russian Federation 115211
    9 Research Site Moscow Moscow/Russia Russian Federation 115280
    10 Research Site Moscow Moscow/Russia Russian Federation 115446
    11 Research Site Moscow Moscow/Russia Russian Federation 115551
    12 Research Site Moscow Moscow/Russia Russian Federation 117042
    13 Research Site Moscow Moscow/Russia Russian Federation 117218
    14 Research Site Moscow Moscow/Russia Russian Federation 117546
    15 Research Site Moscow Moscow/Russia Russian Federation 117556
    16 Research Site Moscow Moscow/Russia Russian Federation 119002
    17 Research Site Moscow Moscow/Russia Russian Federation 119180
    18 Research Site Moscow Moscow/Russia Russian Federation 119607
    19 Research Site Moscow Moscow/Russia Russian Federation 119633
    20 Research Site Moscow Moscow/Russia Russian Federation 121309
    21 Research Site Moscow Moscow/Russia Russian Federation 121374
    22 Research Site Moscow Moscow/Russia Russian Federation 123308
    23 Research Site Moscow Moscow/Russia Russian Federation 124365
    24 Research Site Moscow Moscow/Russia Russian Federation 124489
    25 Research Site Moscow Moscow/Russia Russian Federation 125993
    26 Research Site Moscow Moscow/Russia Russian Federation 127273
    27 Research Site Moscow Moscow/Russia Russian Federation 127642

    Sponsors and Collaborators

    • AstraZeneca

    Investigators

    • Principal Investigator: Olga Pesheva, GBUZ GP # 121 DZM
    • Principal Investigator: Tatyana Yurchak, GBUZ GP # 52 DZM
    • Principal Investigator: Veronika Vovk, GBUZ GP # 2 DZM
    • Principal Investigator: Dmitriy Privalov, GBUZ GKB # 51 DZM
    • Principal Investigator: Maria Klepikova, GBUZ GKB # 13 DZM
    • Principal Investigator: Olga Belkorey, GBUZ GP # 218 DZM
    • Principal Investigator: Natalya Karabinskaya, GBUZ GP # 19 DZM
    • Principal Investigator: Natalya Bosyakova, GBUZ GP # 19 DZM
    • Principal Investigator: Marina Lepatova, GBUZ GP # 107 DZM
    • Principal Investigator: Elena Dorofeeva, FGBU "Polyclinic # 1" Administrative Department of the President of the Russian Federation
    • Principal Investigator: Irina Shoshina, GBUZ GP # 109 DZM
    • Principal Investigator: Darya Semenova, GBUZ GP # 23 DZM
    • Principal Investigator: Elena Zherebetskaya, GBUZ KDC # 2 DZM
    • Principal Investigator: Marina Yarygina, GBUZ GP # 175 DZM
    • Principal Investigator: Elena Lukinskaya, GBUZ GP # 115 DZM
    • Principal Investigator: Irina Borovikova, GBUZ GP # 209 DZM
    • Principal Investigator: Tatiana Sladkova, GBUZ GP # 22 DZM
    • Principal Investigator: Elena Demyanova, GBUZ GP # 64 DZM

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    AstraZeneca
    ClinicalTrials.gov Identifier:
    NCT03654157
    Other Study ID Numbers:
    • D1843R00279
    First Posted:
    Aug 31, 2018
    Last Update Posted:
    Feb 10, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 10, 2022