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Influenza Vaccine To Prevent Adverse Vascular Events:Pilot (IVVE:Pilot)

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
inactivated trivalent influenza vaccine
Sterile saline
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring vascular, influenza, vaccine, heart failure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years and NYHA functional class II, III and IV

Exclusion Criteria:

  • Anaphylactic reaction to a previous dose of TIV
  • Known IgE-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

Sites / Locations

  • Maputo Central Hospital
  • University of Philippines
  • Mulago Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

influenza vaccine

placebo vaccination

Arm Description

Participants at high risk for adverse vascular events will be immunized with 0.5 ml dose of inactivated trivalent influenza vaccine

Participants at high risk for adverse vascular events will be immunized with a 0.5 ml dose of sterile saline inactivated during the influenza season.

Outcomes

Primary Outcome Measures

Feasibility
If no more than 5% of all recruited subjects crossed over from one study group to the other, and if there is at least 98% follow up.

Secondary Outcome Measures

Adverse cardiovascular event
The primary outcome will be a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke and hospitalizations for heart failure using standardized criteria.
Cardiovascular death
CV death alone will be a secondary outcome.

Full Information

First Posted
September 13, 2013
Last Updated
October 25, 2018
Sponsor
McMaster University
Collaborators
Population Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01945268
Brief Title
Influenza Vaccine To Prevent Adverse Vascular Events:Pilot
Acronym
IVVE:Pilot
Official Title
A Randomized Controlled Trial of Influenza Vaccine to Prevent Adverse Vascular Events: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Population Health Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

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. 600 participants will be enrolled prior to influenza season and randomized to either influenza vaccine or saline placebo.
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. This pilot study will provide needed data to establish the feasibility of a larger study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
vascular, influenza, vaccine, heart failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
107 (Actual)

8. Arms, Groups, and Interventions

Arm Title
influenza vaccine
Arm Type
Experimental
Arm Description
Participants at high risk for adverse vascular events will be immunized with 0.5 ml dose of inactivated trivalent influenza vaccine
Arm Title
placebo vaccination
Arm Type
Placebo Comparator
Arm Description
Participants at high risk for adverse vascular events will be immunized with a 0.5 ml dose of sterile saline inactivated during the influenza season.
Intervention Type
Drug
Intervention Name(s)
inactivated trivalent influenza vaccine
Other Intervention Name(s)
VAXIGRIP vaccine
Intervention Description
0.5 ml dose injected intramuscularly
Intervention Type
Other
Intervention Name(s)
Sterile saline
Intervention Description
0.5 ml dose injected intramuscularly
Primary Outcome Measure Information:
Title
Feasibility
Description
If no more than 5% of all recruited subjects crossed over from one study group to the other, and if there is at least 98% follow up.
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Adverse cardiovascular event
Description
The primary outcome will be a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal stroke and hospitalizations for heart failure using standardized criteria.
Time Frame
Six months
Title
Cardiovascular death
Description
CV death alone will be a secondary outcome.
Time Frame
Six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years and NYHA functional class II, III and IV Exclusion Criteria: Anaphylactic reaction to a previous dose of TIV Known IgE-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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Loeb, MD, MSc
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maputo Central Hospital
City
Maputo
Country
Mozambique
Facility Name
University of Philippines
City
Manila
State/Province
Emita
Country
Philippines
Facility Name
Mulago Hospital
City
Kampala
Country
Uganda

12. IPD Sharing Statement

Plan to Share IPD
No
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