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Vaccination Against Influenza to Prevent Cardiovascular Events After Acute Coronary Syndromes (VIP-ACS)

Primary Purpose

Acute Coronary Syndrome

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Double Dose Quadrivalent Influenza Vaccine
Standard Dose Quadrivalent Influenza Vaccine
Sponsored by
Hospital Israelita Albert Einstein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring Unstable angina, Non-ST-Elevation Myocardial Infarction - NSTEMI, ST-Elevation Myocardial Infarction - STEMI, Quadrivalent Influenza Vaccine - QIV

Eligibility Criteria

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

Inclusion Criteria

  • Age >= 18 years and older
  • Acute coronary syndrome in hospital phase.

Exclusion Criteria:

  • Participation in another clinical trial with vaccines;
  • Refusal to provide consent;
  • Hypersensitivity and/or anaphylaxis to any component of the vaccine, or Guillain-Barré within 6 weeks after previous influenza vaccine;
  • Have already received the influenza vaccine with the same strains used in the study within the last 12 months of inclusion in the study
  • Breastfeeding women;
  • Pregnant women;
  • Presenting an acute coronary syndrome during months of December, January, and February.
  • Acute coronary syndrome hospitalization >7 days

Sites / Locations

  • Hospital e Clínica São Roque
  • Hospital Ana Nery
  • Hospital Cárdio Pulmonar
  • Universidade Federal do Ceará / Hospital Universitário Walter Cantídio
  • Instituto de Cardiologia do Distrito Federal
  • Hospital Santa Lucia
  • Hospital Universitário Ciências Médicas
  • Hospital Universitario da Universidade Estadual de Londrina
  • Hospital Agamenon Magalhães
  • Pronto Socorro Cardiológico de Pernambuco
  • Hospital São Lucas da PUCRS
  • Instituto Estadual de Cardiologia Aloysio de Castro
  • Hospital de Clínicas de Porto Alegre
  • IPEMI - Instituto de Pesquisas Médicas de Itajaí
  • Hospital Dona Helena
  • Hospital Regional Hans Dieter Schmidt
  • Centro de Pesquisa Clinica do Coração
  • Faculdade de Medicina de Botucatu - UNESP
  • Irmandade da Santa Casa de Misericórdia de Marília
  • Instituto do Coração - HC FMUSP
  • Santa Casa de Misericórdia de Presidente Prudente
  • Instituto Dante Pazzanese

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Double Dose Quadrivalent Influenza Vaccine

Standard Dose Quadrivalent Influenza Vaccine

Arm Description

Double Dose QIV during index ACS hospitalization

Standard Dose QIV 30 days after randomization

Outcomes

Primary Outcome Measures

Hierarchical composite endpoint consisting of death, myocardial infarction, stroke, unstable angina hospitalization, heart failure hospitalization, urgent coronary revascularization or respiratory infections hospitalizations
The primary objective will be analyzed using the win ratio approach comparing every participant of treatment group to every participant of control group to determine a winner

Secondary Outcome Measures

Key Secondary End Point is a hierarchical outcome consisting only of cardiovascular death, myocardial infarction or stroke.
The key secondary end point will be analyzed using the win ratio approach comparing every participant of treatment group to every participant of control group to determine a winner
Total mortality
Time to first occurrence of all cause death
Cardiovascular mortality
Time to first occurrence of CV death
Myocardial infarction
Time to first occurrence of myocardial infarction
Unstable angina hospitalization
Time to first occurrence of Unstable angina hospitalization
Stroke
Time to first occurrence of stroke
TIA (Transient ischemic attack)
Time to first occurrence of TIA
Heart failure hospitalizations
Time to first occurrence of Heart failure hospitalizations
Respiratory infections hospitalizations
Time to first occurrence of hospitalization due to upper and lower respiratory tract infection (excluding COVID-19)
Need for myocardial revascularization
Time to first occurrence of urgent coronary revascularization ischemia guide (urgent or not-urgent)
Stent thrombosis
Time to first occurrence of probable and definite stent thrombosis
COVID-19 hospitalizations
Time to first occurrence of COVID-19 hospitalizations

Full Information

First Posted
June 26, 2019
Last Updated
August 30, 2022
Sponsor
Hospital Israelita Albert Einstein
Collaborators
Ministry of Health, Brazil
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1. Study Identification

Unique Protocol Identification Number
NCT04001504
Brief Title
Vaccination Against Influenza to Prevent Cardiovascular Events After Acute Coronary Syndromes
Acronym
VIP-ACS
Official Title
Evaluation of the Effectiveness of Double Dose Influenza Vaccination to Reduce Major Cardiovascular Events After an Acute Coronary Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
July 19, 2019 (Actual)
Primary Completion Date
August 28, 2022 (Actual)
Study Completion Date
August 28, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Israelita Albert Einstein
Collaborators
Ministry of Health, Brazil

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Cardiovascular disease has a great burden in the context of public health, as well as the low pharmacological adherence of patients who have chronic non-transmissible diseases. However, the investigators do not have data on the efficacy of vaccination to reduce cardiovascular events in the acute coronary syndromes, and the few studies evaluating the cardioprotective potential of the influenza vaccine were conducted in countries with well defined seasonalities, divergent of Brazil, that presents a constant viral circulation during all months of the year and distinct among its regions. Therefore, study evaluating higher dose vaccination in a period that contemplates the seasonality of the influenza virus in Brazil may bring important findings to different scientific gaps, as well as clarify questions about the possible benefit of doubled vaccination - which does not present contraindications - immediately after a atherothrombotic event. If it shows real benefit, it could also be a future therapeutic tool adjuvant to traditional drug therapy in the prevention of cardiovascular events.
Detailed Description
Phase III, randomized, controlled, multicenter, open-label, superiority, 1:1 allocation, blind assessment of clinical outcomes and intention-to-treat analysis clinical trial to determine whether increased doses(double dose) of influenza vaccine in the hospital phase, when compared to usual dose vaccination (30 days of randomization), decreases the risk of cardiovascular and respiratory events. Hospitalizations due to COVID-19 are excluded from the respiratory infection component of the primary outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome
Keywords
Unstable angina, Non-ST-Elevation Myocardial Infarction - NSTEMI, ST-Elevation Myocardial Infarction - STEMI, Quadrivalent Influenza Vaccine - QIV

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1801 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Double Dose Quadrivalent Influenza Vaccine
Arm Type
Experimental
Arm Description
Double Dose QIV during index ACS hospitalization
Arm Title
Standard Dose Quadrivalent Influenza Vaccine
Arm Type
Active Comparator
Arm Description
Standard Dose QIV 30 days after randomization
Intervention Type
Biological
Intervention Name(s)
Double Dose Quadrivalent Influenza Vaccine
Intervention Description
Double Dose QIV (30µg Hemagglutinin)
Intervention Type
Biological
Intervention Name(s)
Standard Dose Quadrivalent Influenza Vaccine
Intervention Description
Standard Dose QIV (15µg Hemagglutinin)
Primary Outcome Measure Information:
Title
Hierarchical composite endpoint consisting of death, myocardial infarction, stroke, unstable angina hospitalization, heart failure hospitalization, urgent coronary revascularization or respiratory infections hospitalizations
Description
The primary objective will be analyzed using the win ratio approach comparing every participant of treatment group to every participant of control group to determine a winner
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Key Secondary End Point is a hierarchical outcome consisting only of cardiovascular death, myocardial infarction or stroke.
Description
The key secondary end point will be analyzed using the win ratio approach comparing every participant of treatment group to every participant of control group to determine a winner
Time Frame
12 months
Title
Total mortality
Description
Time to first occurrence of all cause death
Time Frame
12 months
Title
Cardiovascular mortality
Description
Time to first occurrence of CV death
Time Frame
12 months
Title
Myocardial infarction
Description
Time to first occurrence of myocardial infarction
Time Frame
12 months
Title
Unstable angina hospitalization
Description
Time to first occurrence of Unstable angina hospitalization
Time Frame
12 months
Title
Stroke
Description
Time to first occurrence of stroke
Time Frame
12 months
Title
TIA (Transient ischemic attack)
Description
Time to first occurrence of TIA
Time Frame
12 months
Title
Heart failure hospitalizations
Description
Time to first occurrence of Heart failure hospitalizations
Time Frame
12 months
Title
Respiratory infections hospitalizations
Description
Time to first occurrence of hospitalization due to upper and lower respiratory tract infection (excluding COVID-19)
Time Frame
12 months
Title
Need for myocardial revascularization
Description
Time to first occurrence of urgent coronary revascularization ischemia guide (urgent or not-urgent)
Time Frame
12 months
Title
Stent thrombosis
Description
Time to first occurrence of probable and definite stent thrombosis
Time Frame
12 months
Title
COVID-19 hospitalizations
Description
Time to first occurrence of COVID-19 hospitalizations
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Solicited injection site and systemic events, unsolicited adverse events and serious adverse events following vaccination.
Description
Occurrence of solicited injection site (Pain, Erythema, Swelling, Induration, and Bruising) and systemic reactions (Fever, Headache, Malaise, Myalgia, and Shivering) will be assessed in all participants.
Time Frame
Day 0 up to Day 7 post-vaccination
Title
Safety overview after influenza vaccination until the end of the study.
Description
Occurrence of unsolicited adverse events, including serious adverse events.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Age >= 18 years and older Acute coronary syndrome in hospital phase. Exclusion Criteria: Participation in another clinical trial with vaccines; Refusal to provide consent; Hypersensitivity and/or anaphylaxis to any component of the vaccine, or Guillain-Barré within 6 weeks after previous influenza vaccine; Have already received the influenza vaccine with the same strains used in the study within the last 12 months of inclusion in the study Breastfeeding women; Pregnant women; Presenting an acute coronary syndrome during months of December, January, and February. Acute coronary syndrome hospitalization >7 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Otávio Berwanger, MD-PhD
Organizational Affiliation
Academic Research Organization -- Hospital Israelita Albert Einstein
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Henrique A Fonseca, PhD
Organizational Affiliation
Academic Research Organization -- Hospital Israelita Albert Einstein
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital e Clínica São Roque
City
Ipiaú
State/Province
Bahia
Country
Brazil
Facility Name
Hospital Ana Nery
City
Salvador
State/Province
Bahia
Country
Brazil
Facility Name
Hospital Cárdio Pulmonar
City
Salvador
State/Province
Bahia
Country
Brazil
Facility Name
Universidade Federal do Ceará / Hospital Universitário Walter Cantídio
City
Fortaleza
State/Province
Ceará
Country
Brazil
Facility Name
Instituto de Cardiologia do Distrito Federal
City
Brasilia
State/Province
DF
Country
Brazil
Facility Name
Hospital Santa Lucia
City
Poços De Caldas
State/Province
MG
Country
Brazil
Facility Name
Hospital Universitário Ciências Médicas
City
Belo Horizonte
State/Province
Minas Gerais
Country
Brazil
Facility Name
Hospital Universitario da Universidade Estadual de Londrina
City
Londrina
State/Province
Paraná
Country
Brazil
Facility Name
Hospital Agamenon Magalhães
City
Recife
State/Province
Pernambuco
Country
Brazil
Facility Name
Pronto Socorro Cardiológico de Pernambuco
City
Recife
State/Province
PE
Country
Brazil
Facility Name
Hospital São Lucas da PUCRS
City
Porto Alegre
State/Province
Rio Grande Do Sul
Country
Brazil
Facility Name
Instituto Estadual de Cardiologia Aloysio de Castro
City
Rio De Janeiro
State/Province
RJ
Country
Brazil
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
RS
Country
Brazil
Facility Name
IPEMI - Instituto de Pesquisas Médicas de Itajaí
City
Itajaí
State/Province
Santa Catarina
Country
Brazil
Facility Name
Hospital Dona Helena
City
Joinville
State/Province
Santa Catarina
Country
Brazil
Facility Name
Hospital Regional Hans Dieter Schmidt
City
Joinville
State/Province
Santa Catarina
Country
Brazil
Facility Name
Centro de Pesquisa Clinica do Coração
City
Aracaju
State/Province
Sergipe
Country
Brazil
Facility Name
Faculdade de Medicina de Botucatu - UNESP
City
Botucatu
State/Province
SP
Country
Brazil
Facility Name
Irmandade da Santa Casa de Misericórdia de Marília
City
Marília
State/Province
SP
Country
Brazil
Facility Name
Instituto do Coração - HC FMUSP
City
São Paulo
State/Province
SP
Country
Brazil
Facility Name
Santa Casa de Misericórdia de Presidente Prudente
City
Presidente Prudente
State/Province
São Paulo
Country
Brazil
Facility Name
Instituto Dante Pazzanese
City
São Paulo
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
36030400
Citation
Fonseca HAR, Furtado RHM, Zimerman A, Lemos PA, Franken M, Monfardini F, Pedrosa RP, Patriota RLS, Passos LCS, Dall'Orto FTC, Hoffmann Filho CR, Nascimento BR, Baldissera FA, Pereira CAC, Caramori PRA, de Andrade PB, Esteves C, Salim EF, da Silva JH, Pedro IC, Silva MCR, de Pedri EH, Carioca ACRD, de Piano LPA, Albuquerque CSN, Moia DDF, Momesso RGRAP, Machado FP, Damiani LP, Soares RVP, Schettino GP, Rizzo LV, Nicolau JC, Berwanger O. Influenza vaccination strategy in acute coronary syndromes: the VIP-ACS trial. Eur Heart J. 2022 Nov 1;43(41):4378-4388. doi: 10.1093/eurheartj/ehac472.
Results Reference
derived

Learn more about this trial

Vaccination Against Influenza to Prevent Cardiovascular Events After Acute Coronary Syndromes

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