Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

ObseRvation After Acute Coronary Syndrome for deveLopment of trEatment Options (ORACLE)

28. august 2019 oppdatert av: Larisa Minushkina, Central State Medical Academy

Exacerbation of Coronary Heart Disease: the Logic and Probabilistic Processes of Flow Prediction for Optimization of Treatment

The aim of the study is developing an individualized risk model for the unfavorable outcomes of coronary artery disease and complications from ongoing therapy, according to clinical, instrumental, biochemical and genetic parameters in patients with acute coronary syndrome.

Inclusion criteria: patients with acute coronary syndrome (with or without ST elevation) who have indications for PCI Number of inclusion patients - 1655 patients Scheduled time of follow up - 24 month Primary end-point: all-cause death Secondary end-points: any cardiovascular events (cardiovascular death, nonfatal myocardial infarction, non-fatal stroke); non-fatal myocardial infarction; recurrent acute coronary syndrome; non-fatal stoke; complicated atherosclerosis; recurrent PCI; bleeding

Studieoversikt

Status

Ukjent

Detaljert beskrivelse

The role of genetic factors in the development of coranary heart disease (CHD) exacerbations studied not enough. Most research in this area planned and carried out on a "case-control". Using a similar protocol entails significant errors are associated with a high incidence of subclinical atherosclerotic vascular lesions. Moreover, much of atheroma is extravasal, making it impossible to identify them by angiography. Therefore, necessary to conduct prospective studies to estimate the frequency of so-called hard endpoints. Previously, similar trials were conducted, mainly in connect with drug approving procedures. The spread data from them to other patients directly is not entirely justified. At the same time, the influence of genetic factors in this group of patients can be substantial.

In the previous part of the study, the sample of patients of Moscow, St. Petersburg, Kazan, Chelyabinsk, Stavropol, Perm, and Rostov-on-the-Don was formed, of 1,200 people admitted due to acute coronary syndrome (ACS) including unstable angina and acute myocardial infarction, at coronary care units with follow-up for three years. We found several factors, including genetic, that significantly affect the outcomes of the disease. Coronary atherosclerosis and its complications now considered as a multifactorial disease associated with inherent factors. Therefore, the project provides, besides accounting a significant amount of clinical and instrumental data, the determination of a wide range of genotypes and alleles of polymorphic markers candidate genes encoding the protein factors of the hemostatic system, enzymes of lipid metabolism system, and anti-inflammatory cytokines. It is assumed that the prediction outcomes of coronary heart disease should be carried out taking into account the fact that several factors (gender, diabetes, age, aortic stenosis, atrial fibrillation, etc.) can not only significantly change the forecast itself but also affecting the significance of other risk factors. Since the last study, the standards significantly of ACS management changed. Invasive treatment not only creates opportunities to reduce coronary mortality but also increased demands on the patient's adherence to the assigned medication and creates additional risks associated with its activity (especially with an antithrombotic treatment activity). In these circumstances, the development of personalized approaches to prescribing drugs is particularly important. Thus, the prediction of coronary heart disease outcomes after an ACS on a set of clinical, instrumental, biochemical and genetic indicators is of great importance, as it allows to plan the most optimal treatment for the individual patient.

The aim of the study was to develop a model of individualized risk of coronary heart disease outcomes and side effects of therapy based on clinical and instrumental, biochemical, and genetic parameters in patients with ACS.

Studietype

Observasjonsmessig

Registrering (Faktiske)

1655

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

Study population consists of consistently hospitalized patients with ACS from 4 vascular centers of Moscow, Kazan, Astrakhan and Krasnodar

Beskrivelse

Inclusion Criteria:

  1. Patients with acute coronary syndrome without ST-segment elevation meeting the criteria of a very high, high or intermediate risk, and patients from the low-risk group, if they have episodes of myocardial ischemia in any way Very high risk (1 criterion is sufficient)

    • Pulmonary edema, most probably due to ischemia.
    • The newly appears or increased noise of mitral regurgitation.
    • Rhythm of the gallop, newly developed or intensified wheezing in the lungs.
    • Hypotension against ischemia
    • Ischemia refractory to treatment
    • Persistent ventricular tachycardia or the occurrence of ventricular rhythm disturbances during an attack of ischemia High risk

      (1 criterion is sufficient)

    • An anginal attack more than 20 minutes within the next 48 hours before admission
    • Transitional elevations ST (duration less than 20 min)
    • GRACE score > 140 points
    • Increased cardiospecific markers of necrosis. (you must have at least 2 criteria)
    • Age> 75 years.
    • Angina pectoris with transient changes ST> 0.05 mV.

    Intermediate risk (1 criterion is sufficient)

    • Age> 75 years.
    • Angina pectoris with transient changes ST> 0.05 mV.
    • Inversion of the T wave on ECG (≥ 0.2 mV).
    • GRACE score 104-139 points

    (it is necessary to have at least 2 criteria)

    • Angina of rest (<20 min), stopped spontaneously or with the help of nitroglycerin (NG).
    • Anamnesis of pathology of peripheral or cerebral arteries,
    • Postponed myocardial infarction, including painless, history of revascularization (PCI or CABG)
    • Diabetes.
    • Chronic renal failure (GFR <50 mL / min)

    Low risk All other patients with suspicion of ACS require a survey to identify episodes of ischemia

  2. Patients with acute coronary syndrome with ST-segment elevation

    Patients who were hospitalized with symptoms due to acute myocardial infarction (the duration of infarction is no more than 10 days, by the time of hospitalization) and at least one of the following additional criteria identified upon admission to hospital:

    • ST elevation: a persistent ST increase of 1 mm in two adjacent leads from the limbs, or an ST increase of 2 mm in two adjacent thoracic leads
    • the appearance of a new left bundle branch block
    • dynamics of acute myocardial infarction
  3. Signed informed consent to participate in the study

Exclusion Criteria:

  • Lack of patient consent to participate in the study
  • Impossibility of contact with the patient after discharge after index event

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: Kohort
  • Tidsperspektiver: Potensielle

Kohorter og intervensjoner

Gruppe / Kohort
acute coronary syndrome
All patients should receive standard therapy for acute coronary syndrome and concomitant diseases. All drugs are prescribed according current guidelines and approved indications.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
all-cause death
Tidsramme: Number of Participants with end-point during 360 days
death from any cause
Number of Participants with end-point during 360 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
cardiovascular events
Tidsramme: Number of Participants with end-point during 360 days
cardiovascular death, non-fatal myocardial infarction, non-fatal stroke
Number of Participants with end-point during 360 days
non-fatal myocardial infarction
Tidsramme: Number of Participants with end-point during 360 days
non-fatal myocardial infarction
Number of Participants with end-point during 360 days
recurrent acute coronary syndrome
Tidsramme: Number of Participants with end-point during 360 days
all cases of recurrent myocardial infarction or unstable angina after the index events
Number of Participants with end-point during 360 days
recurrent PCI
Tidsramme: Number of Participants with end-point during 360 days
all cases of recurrent PCI after the index hospitalization
Number of Participants with end-point during 360 days
complicated atherosclerosis
Tidsramme: Number of Participants with end-point during 360 days
peripheral atherosclerosis need hospitalisation
Number of Participants with end-point during 360 days
non-fatal stroke
Tidsramme: Number of Participants with end-point during 360 days
all cases of non-fatal stroke
Number of Participants with end-point during 360 days

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
bleeding
Tidsramme: Number of Participants with end-point during 360 days
all cases of bleeding during and after the index hospitalization
Number of Participants with end-point during 360 days

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Dmitry A Zateyshchikov, prof, Central State Medical Academy

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

5. november 2014

Primær fullføring (Faktiske)

20. februar 2018

Studiet fullført (Forventet)

20. februar 2020

Datoer for studieregistrering

Først innsendt

20. august 2019

Først innsendt som oppfylte QC-kriteriene

22. august 2019

Først lagt ut (Faktiske)

28. august 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. august 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

28. august 2019

Sist bekreftet

1. august 2019

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

Nei

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Akutt koronarsyndrom

3
Abonnere