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Clinical Trial ● Currently Recruiting Phase IV NCT06336317

Effect of infLuenza vaccInation After Myocardial INfArction on Cardiac inflammaTory responsE

Effect of infLuenza vaccInation After Myocardial INfArction on Cardiac inflammaTory responsE — Recruiting • Phase IV • Cardiology / Cardiovascular • NCT06336317.

📅 07 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase IV
NCT ID
NCT06336317
Sponsor
Region Örebro County
Start
2024-04-24
ClinicaliQ Trial Snapshot
  • Effect of infLuenza vaccInation After Myocardial INfArction on Cardiac inflammaTory responsE — Recruiting • Phase IV • Cardiology / Cardiovascular • NCT06336317.
  • The goal of this randomized, double-blind, placebo-controlled clinical trial is to investigate the immunological effects of influenza vaccination outside of the influenza season on arterial inflammation in patients with a recent acute myocardial infarction (AMI). The primary objective is to compare the….
  • Sponsor: Region Örebro County.

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What This Trial Is Studying

The goal of this randomized, double-blind, placebo-controlled clinical trial is to investigate the immunological effects of influenza vaccination outside of the influenza season on arterial inflammation in patients with a recent acute myocardial infarction (AMI). The primary objective is to compare the effects of influenza vaccination to those of a placebo in reducing post-myocardial infarction coronary inflammation as measured by coronary computed tomography angiography (CCTA). The main questions it aims to answer are: Does influenza vaccination reduce arterial inflammation as measured by CCTA at week 8 after percutaneous coronary intervention…

Eligibility Snapshot
  • : * Patients with a diagnosis of non-ST-segment elevation myocardial infarction * A finalized coronary PCI * Male or non-fertile female subjects ≥18 years. (Females without childbearing potential, postmenopausal women and women with a history of hysterectomy or other medical conditions that preclude pregnancy) * Written informed consent * A CCTA can be scheduled within 7 days after PCI

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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