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NCT06058182Recruiting

RNA as Prognostic Biomarkers in Patients With Acute Coronary Syndrome

Source: ClinicalTrials.gov · Last updated 6 Oct 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Identify circulating protein-coding (mRNAs) or non-coding (ncRNAs) transcripts (ACS\_signature) predictive of ventricular dysfunction in ACS patients undergoing PCI.

Status (registry)
Recruiting
Study type
Observational
Enrollment
70 (estimated)
First submitted
15 Feb 2023
Start date
13 Jul 2020
Primary completion date
30 Jan 2026
Lead sponsor
IRCCS Policlinico S. Donato
NCT number
NCT06058182

What you commit to

  • Study type: Observational
  • Planned participants: 70
  • From 13 Jul 2020 to the primary completion date, 30 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous cardiac surgery including coronary artery bypass grafts
  • Any contraindication to drug-eluting stent implantation (DES)

Other illness

  • Severe valve disease or other conditions requiring cardiac surgery
  • Patients with known hypersensitivity or contraindication to any of the following drugs:
    • heparin
    • aspirin,
    • clopidogrel,
    • ticlopidine,
    • sirolimus,
    • everolimus.
  • Patients with a documented history of myocardial infarction;
  • Patients with advanced ST-segment elevation myocardial infarction (\> 48 h from onset of symptoms/Q waves on electrocardiogram) or undergoing fibrinolysis;
  • Patients with malignant neoplasm or systemic disease with quoad vitam prognosis less than 1 year;
  • Patients with known active infectious diseases;

Lab values

  • Left ventricular ejection fraction (LVEF) \<30% before PCI
  • Patients with prior known cardiomyopathy with LVEF \< 40%

Other

  • Total chronic occlusions
  • Patients in cardiogenic shock
  • Patients who are unable to express valid informed consent to the act of enlistment
  • Pregnant women

Who the study is looking for

  • Age \>18 years
  • Patients with ACS (first episode), defined according to the guidelines of the European Society of Cardiology (ESC) 2017
  • Indication for percutaneous revascularization treatment
  • Informed consent to study enrollment

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS Policlinico S. Donato, Milan, Italy
Coordinator of this site? Confirm its status
MilanItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.