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Influenza Vaccine To Prevent Adverse Vascular Events (RCT-IVVE)

A Randomized Controlled Trial of Influenza Vaccine to Prevent Adverse Vascular Events

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02762851
Acronym
RCT-IVVE
Enrollment
5000
Registered
2016-05-05
Start date
2016-06-30
Completion date
2020-12-31
Last updated
2018-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Influenza

Keywords

Influenza, Vaccine, Heart failure, Vascular

Brief summary

A multi-centre, randomized, placebo controlled, trial. Participants at high-risk for vascular events from the network of INTER- CHF will be randomized to inactivated influenza vaccine or placebo and followed prospectively over three influenza seasons. 5,000 participants will be enrolled prior to influenza season, randomized to either influenza vaccine or saline placebo, either of which they will receive annually for three years and then followed over each of the influenza seasons.

Detailed description

Cardiovascular disease is a major cause of morbidity and mortality. There is recent evidence that infection due to influenza may precipitate vascular events such as myocardial infarctions and strokes. There is some evidence that influenza vaccination may prevent such events but the data are inconclusive. The investigators propose a randomized controlled trial to assess whether influenza vaccination will prevent vascular illness. Adults with clinical heart failure will be randomized to inactivated influenza vaccine or saline placebo each year for three consecutive years. They will be followed over six months for a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke and hospitalizations for heart failure using standardized criteria. Rigorous demonstration of influenza vaccine leading to a reduction in major adverse vascular events in patients with heart failure would lead to a major change in how these patients are managed. Given the large burden of disease both in Canada and globally, the possibility to reduce cardiovascular and stroke related death is a compelling reason to conduct this trial.

Interventions

OTHERSterile saline

0.5 ml dose injected intramuscularly

0.5 ml dose injected intramuscularly

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years and NYHA (New York Heart Association) functional class II, III and IV

Exclusion criteria

* Anaphylactic reaction to a previous dose of TIV(trivalent influenza vaccine) * Known IgE( Immunoglobulin E)-mediated hypersensitivity to eggs manifested as hives, swelling of the mouth and throat, difficulty in breathing, hypotension, or shock * Guillain-Barré syndrome within eight weeks of a previous influenza vaccine * Anaphylactic reaction to neomycin * Patients who have had influenza vaccine in two of the three previous years

Design outcomes

Primary

MeasureTime frameDescription
Adverse cardiovascular eventSix monthsThe primary outcome will be a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke and hospitalizations for heart failure using standardized criteria.

Secondary

MeasureTime frameDescription
Cardiovascular (CV) deathSix monthsCV death alone will be a secondary outcome.

Countries

Cameroon, China, India, Kenya, Lebanon, Mozambique, Nigeria, Philippines, Saudi Arabia, Sudan, Uganda, United Arab Emirates, Zambia

Contacts

Primary ContactMark Loeb, MD, MSc.
loebm@mcmaster.ca905-525-9140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026