Registry of Acute Coronary Syndrome in the Regional Cardiovascular Center (NCT06845384) | Clinical Trial Compass
CompletedNot Applicable
Registry of Acute Coronary Syndrome in the Regional Cardiovascular Center
Russia555 participantsStarted 2025-01-15
Plain-language 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.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. 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.
Exclusion criteria
. 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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This registry study tracked all-cause mortality in people with acute coronary syndrome — can you tell me what the main findings were and whether they're relevant to my specific situation?
2Since this was an observational registry rather than a treatment trial, does the data collected here influence how you'd approach my care, or are there active treatment trials I should also be asking about?
3The study is already completed — is there any published data or results from this registry that we could look at together to better understand outcomes for people with my type of acute coronary syndrome?
4Because this was a registry study with no assigned treatment, what does 'standard of care' look like for acute coronary syndrome at a regional cardiovascular center, and is that what I'd be receiving?
5Are there ongoing or upcoming trials based on what this registry found that might be worth considering as a next step in my care?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
all-cause mortality
Timeframe: 1 year and 3 years
Trial details
NCT IDNCT06845384
SponsorNational Medical Research Center for Therapy and Preventive Medicine