Ignite Creation Date:
2025-12-24 @ 3:23 PM
Ignite Modification Date:
2025-12-26 @ 1:03 AM
Study NCT ID:
NCT05232292
Status:
UNKNOWN
Last Update Posted:
2022-02-09
First Post:
2021-12-19
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Influenza Vaccination During Coronavirus Disease 2019 Outbreak After Acute Coronary Syndrome and Chronic Heart Failure
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D054058', 'term': 'Acute Coronary Syndrome'}, {'id': 'D007251', 'term': 'Influenza, Human'}], 'ancestors': [{'id': 'D017202', 'term': 'Myocardial Ischemia'}, {'id': 'D006331', 'term': 'Heart Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D012141', 'term': 'Respiratory Tract Infections'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D009976', 'term': 'Orthomyxoviridae Infections'}, {'id': 'D012327', 'term': 'RNA Virus Infections'}, {'id': 'D014777', 'term': 'Virus Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 200}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2021-10-06', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-01', 'completionDateStruct': {'date': '2023-05-31', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2022-01-30', 'studyFirstSubmitDate': '2021-12-19', 'studyFirstSubmitQcDate': '2022-01-30', 'lastUpdatePostDateStruct': {'date': '2022-02-09', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-02-09', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2022-12-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Primary endpoint', 'timeFrame': 'up to 1 year', 'description': 'сomposite of all-cause death, MI, or stent thrombosis at 12 months'}], 'secondaryOutcomes': [{'measure': 'Secondary endpoint', 'timeFrame': 'up to 1 year', 'description': 'The number of participants with all-cause death and myocardial infarction till 1 year'}, {'measure': 'Secondary endpoint', 'timeFrame': '1 week after vaccination', 'description': 'Safety of vaccination (incidence of side effects)'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['acute coronary syndrome', 'influenza vaccination', 'prognosis', 'chronic heart failure'], 'conditions': ['Acute Coronary Syndrome', 'Chronic Heart Failure']}, 'descriptionModule': {'briefSummary': 'Study Description:\n\nBackground: Well-known fact that the number of cardiovascular diseases is on the rise during influenza epidemic. It is conceivable that influenza may precipitate plaque rupture, increase cytokines with central roles in plaque destabilization and trigger the coagulation cascade. A number of studies have shown that the risk of cardiovascular complications (ACS, stroke, CHF decompensation, cardiac arrhythmias) seem to be reduced following influenza vaccination. The Influenza Vaccination After Myocardial Infarction study data published in September 2021 have demonstrated a significant decrease of mortality (by 40%) during 1 year of follow-up in patients with myocardial infarction (MI) who has been vaccinated during the first 72 hours.\n\nObjective: the objective is to find out whether influenza vaccination protects against cardiovascular events and death in ACS \\& CHF patients vaccinated during hospitalization Methods: Population: 400 patients aged 65 and older with acute coronary syndrome are randomized 1:1 and followed up via telephone calls and registries (AIS "Mortality").\n\nPatients will be included in the study in cardiology departments № 1, 2, 3, 5, 6 of the State Budgetary Healthcare Institution "Samara Regional Clinical Cardiology Dispensary named after V.P. Polyakov" Intervention: Influenza vaccination. Control: group of unvaccinated patients. Planned study period is 1 year.', 'detailedDescription': 'Detailed Description:\n\nName of investigational treatment: Influenza vaccine ("Ultrix Quadri"™) Planned study period: October - December 2021 ((influenza season) Long-term follow up to 365 days from the moment of vaccination of the last included patient (approximately November-December 2022) via phone calls.\n\nMethodology: vaccination will be start after informed consent on the day of leaving hospital with "Ultrix Quadri"™ vaccine Intervention Model: Parallel Assignment Number of subjects: 400 Number of vaccinated patients is 200 Number of patients with placebo is 200 Primary endpoint: сomposite of all-cause death, MI, or stent thrombosis at 12 months Secondary endpoints\n\n* The number of participants with all-cause death till 1 year (key secondary outcome)\n* The number of participants with myocardial infarction till 1 year (key secondary outcome)\n* The number of participants with stent thrombosis till 1 year (key secondary outcome)\n* The number of participants with cardiovascular death till 1 year (key secondary outcome)\n* The number of participants with a new revascularization till 1 year\n* The number of participants with cardiovascular death, a new myocardial infarction or stent thrombosis (first occurring) till 1 year\n* The number of participants with stroke, including transient ischemic attack (TIA) till 1 year\n* The number of participants with hospitalization for heart failure till 1 year\n* The number of participants with hospitalization for arrhythmia till 1 year\n* Safety of vaccination (incidence of side effects)\n\nFollow up by telephone and registry information (AIS "Mortality"): the follow up for endpoints will be performed using telephone contacts with the patients or first degree relatives.\n\nPurpose of phone calls:\n\n* to assess the safety of vaccination the day after vaccination (T1) 7 (± 1) day after vaccination (T2)\n* to study the effectiveness 365 (± 5) days after vaccination (T3)\n\nReporting for adverse events: The patients will be informed to contact the investigator or study nurse if any adverse event should occur during this timeframe.\n\nStudy Start Date: September 2021 Actual Primary Completion Date (safety assessment): December 2021 Actual Study Completion Date (efficiency mark): December 2022 Experimental Drug: influenza vaccine Ultrix Quadri Standard influenza vaccine administered as a deep subcutaneous injection at one occasion per subject.\n\nThe experimental drug is not administered to patients in the control group.\n\nEligibility Criteria:\n\nAges Eligible for Study: 65 Years and older (Adult, Older Adult) Sexes Eligible for Study: All\n\nInclusion Criteria:\n\n* Patients with a diagnosis of ACS with transformation to acute MI or unstable angina Patients with a diagnosis of Chronic Heart Failure due to different reasons\n* Written informed consent.\n\nExclusion Criteria:\n\n* Influenza vaccination during the current influenza season or anticipating to be vaccinated during the current influenza season.\n* Coronavirus disease 2019 vaccination during 30 days\n* Indication for influenza vaccination for some indication other than myocardial infarction.\n* Severe allergy to eggs or previous allergic reaction to influence vaccine.\n* Suspicion of febrile illness or acute, ongoing infection.\n* Hypersensitivity to the active substances or ingredients of Ultrix Quadri or against any residues, such as eggs (ovalbumin or chicken proteins), neomycin, formaldehyde and octoxinol.\n* Subjects with endogenic or iatrogenic immunosuppression that may result in reduced immunization response.\n* Inability to provide informed consent.\n* Age below 65 years.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['OLDER_ADULT'], 'minimumAge': '65 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Patients with a diagnosis of ACS with transformation to AMI or unstable angina\n* Patients with a diagnosis of CHF Written informed consent.\n\nExclusion Criteria:\n\n* • Influenza vaccination during the current influenza season or anticipating to be vaccinated during the current influenza season.\n\n * COVID-19 vaccination during 30 days\n * Indication for influenza vaccination for some indication other than myocardial infarction.\n * Severe allergy to eggs or previous allergic reaction to influence vaccine.\n * Suspicion of febrile illness or acute, ongoing infection.\n * Hypersensitivity to the active substances or ingredients of Ultrix Quadri or against any residues, such as eggs (ovalbumin or chicken proteins), neomycin, formaldehyde and octoxinol.\n * Subjects with endogenic or iatrogenic immunosuppression that may result in reduced immunization response.\n * Inability to provide informed consent.\n * Age below 65 years.'}, 'identificationModule': {'nctId': 'NCT05232292', 'acronym': 'IV-ACS&CHF', 'briefTitle': 'Influenza Vaccination During Coronavirus Disease 2019 Outbreak After Acute Coronary Syndrome and Chronic Heart Failure', 'organization': {'class': 'OTHER', 'fullName': 'Samara Regional Cardiology Dispensary'}, 'officialTitle': 'Influenza Vaccination During COVID19 Outbreak After Acute Coronary Syndrome and Chronic Heart Failure', 'orgStudyIdInfo': {'id': 'SOKKD003'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'Vaccinated', 'description': 'vaccinated ACS \\& CHF patients over 65 years', 'interventionNames': ['Biological: Ultrix Quadri']}, {'type': 'NO_INTERVENTION', 'label': 'Not vaccinated', 'description': 'not vaccinated ACS \\& CHF patients over 65 years'}], 'interventions': [{'name': 'Ultrix Quadri', 'type': 'BIOLOGICAL', 'description': 'vaccination by Ultrix Quadri against flu', 'armGroupLabels': ['Vaccinated']}]}, 'contactsLocationsModule': {'locations': [{'zip': '443070', 'city': 'Samara', 'status': 'RECRUITING', 'country': 'Russia', 'contacts': [{'name': 'Dmitry Duplyakov, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Samara Regional Cardiology Dispansery', 'geoPoint': {'lat': 53.20767, 'lon': 50.13553}}], 'centralContacts': [{'name': 'Dmitry Duplyakov, Prof', 'role': 'CONTACT', 'email': 'duplyakov@yahoo.com', 'phone': '89277297273'}], 'overallOfficials': [{'name': 'Dmitry Duplyakov, Prof', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'SOKKD'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Samara Regional Cardiology Dispensary', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Medical Director', 'investigatorFullName': 'Prof. Dmitry Duplyakov FESC', 'investigatorAffiliation': 'Samara Regional Cardiology Dispensary'}}}}