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A Prospective, Single-center, Observational Study Aiming to Assess the Predictive Role of Flow Mediated Dilatation in Acute Coronary Syndromes, Combined With Echocardiographic and Biochemical Indices: The Novel Cor-IS Technology Will Also be Evaluated (FLARE-ACS)

A

Aristotle University Of Thessaloniki

Status

Enrolling

Conditions

Acute Coronary Syndromes
Endothelial Function (FMD)
Flow Mediated Dilation

Treatments

Diagnostic Test: Observation group

Study type

Observational

Funder types

Other

Identifiers

NCT06890013
198/31.5.2024

Details and patient eligibility

About

A prospective, single-center, observational study aiming to assess the predictive role of flow mediated dilatation in acute coronary syndromes, combined with echocardiographic and biochemical indices. The novel Cor-IS technology will also be evaluated.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age > 18 years
  2. Patients hospitalized due to acute coronary syndrome (STEMI, NSTEMI)
  3. Capability of providing written informed consent
  4. Patients able to comply with the follow-up schedule of the study

Exclusion criteria

  1. Patients with acute coronary syndromes classified as MINOCA, or type II myocardial infarction
  2. Patients with rare acute coronary syndrome types, such as spontaneous coronary artery dissection or Takotsubo syndrome
  3. Patients with congenital heart disease
  4. Age > 85 years
  5. Patients with end stage chronic kidney disease
  6. Patients with active malignancy or autoimmune diseases which limit their survival
  7. Patients with expected survival < 1 year due to other reasons
  8. Suboptimal echocardiographic windows
  9. Inability to provide written consent
  10. Inability to comply with the follow-up schedule of the study
  11. Pregnancy
  12. Use of intravenous drugs

Trial design

100 participants in 1 patient group

Observation group
Description:
Patients hospitalized due to acute coronary syndromes (STEMI, NSTEMI)
Treatment:
Diagnostic Test: Observation group

Trial contacts and locations

1

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Central trial contact

Christodoulos E. Papadopoulos, PhD; Georgios Zormpas, MD

Data sourced from clinicaltrials.gov

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