Registry of Acute Coronary Syndrome in the Regional Cardiovascular Center
STOCS
1 other identifier
observational
300
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 15, 2025
CompletedFirst Submitted
Initial submission to the registry
February 20, 2025
CompletedFirst Posted
Study publicly available on registry
February 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2026
CompletedMarch 3, 2025
February 1, 2025
1 year
February 20, 2025
February 26, 2025
Conditions
Keywords
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
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
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Sergey Martsevich, D.M., professor
National Medical Research Centre for Therapy and Preventive Medicine, Moscow, Russia
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