NCT06845384

Brief Summary

The study is a prospective registry of patients consequently admitted to the regional cardiovascular center with a diagnosis of acute coronary syndrome, in order to study the behavior of patients from the first minutes of the onset of the anginal syndrome, and influence of the delay in calling of ambulance on short-term and long-term outcomes of the disease. Other factors which may influence short-term and long-term outcomes will also be assessed.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

February 20, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 25, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2026

Completed
Last Updated

March 3, 2025

Status Verified

February 1, 2025

Enrollment Period

1 year

First QC Date

February 20, 2025

Last Update Submit

February 26, 2025

Conditions

Keywords

acute coronary syndromepercutaneous coronary interventionunstable anginaacute myocardial infarction

Outcome Measures

Primary Outcomes (1)

  • all-cause mortality

    1 year and 3 years

Secondary Outcomes (1)

  • Сombined secondary end-point

    1 year and 3 years

Study Arms (1)

No

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients consequently admitted to the regional cardiovascular center with a diagnosis of acute coronary syndrome, in order to study the behavior of patients from the first minutes of the onset of the anginal syndrome, and influence of the delay in calling of ambulance on short-term and long-term outcomes of the disease.

You may qualify if:

  • Men and women aged 18 and over, permanently residing in the Moscow region and in Moscow.
  • Patients hospitalized in the Regional Vascular Center of Stupino Clinical Hospital (GBUZ MO SKB) with a diagnosis of ACS with and without ST-segment elevation.
  • Signing an informed consent form to participate in the study and the processing of personal data, as well as conducting a telephone survey during the follow-up.

You may not qualify if:

  • The patient's refusal to participate in the study and to allow the use of personal data during the study.
  • The presence of mental illness.
  • The patient plans to leave Russia for permanent or long-term residence.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Medical Research Centre for Therapy and Preventive Medicine

Moscow, 101990, Russia

Location

MeSH Terms

Conditions

Acute Coronary SyndromeAngina, Unstable

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesAngina PectorisChest PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Sergey Martsevich, D.M., professor

    National Medical Research Centre for Therapy and Preventive Medicine, Moscow, Russia

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 20, 2025

First Posted

February 25, 2025

Study Start

January 15, 2025

Primary Completion

January 15, 2026

Study Completion

January 15, 2026

Last Updated

March 3, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Locations