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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06029933
Other study ID # 2033496
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 17, 2023
Est. completion date May 2026

Study information

Verified date September 2023
Source Kaiser Permanente
Contact Amber H. Hyman, PhD, MPH
Phone 510-267-7571
Email Amber.Hyman@kp.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will evaluate the relative vaccine effectiveness of quadrivalent adjuvanted inactivated influenza vaccine (aIIV4) versus quadrivalent high-dose inactivated influenza vaccine (HD-IIV4) in preventing polymerase chain reaction (PCR)-confirmed influenza and influenza-related outcomes in adults ≥65 years of age during the 2023/24 and 2024/25 influenza seasons. The study is an observational study conducted at Kaiser Permanente Northern California (KPNC), an integrated health care system in the United States.


Recruitment information / eligibility

Status Recruiting
Enrollment 960000
Est. completion date May 2026
Est. primary completion date May 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Age =65 years at the time of influenza vaccination - KPNC member at the time of vaccination - Receive either aIIV4 or HD-IIV4 at a KPNC facility during the 2023/24 and/or 2024/25 influenza seasons Exclusion Criteria: - Age <65 years at the time of influenza vaccination - Received either aIIV4 or HD-IIV4 in the inpatient setting - Receive more than one influenza vaccination during a single season period (i.e., 2023/24 or 2024/25 influenza seasons) - Receive an influenza vaccination outside of KPNC

Study Design


Intervention

Biological:
Adjuvanted Quadrivalent Inactivated Influenza Vaccine (aIIV4)
Fluad Quadrivalent vaccine is an inactivated influenza vaccine formulated to contain 60 mcg of hemagglutinin (HA) total, with 15 mcg from each of the four recommended influenza strains and the MF59 adjuvant in single-dose prefilled 0.5 mL syringes. Kaiser Permanente Northern California members =65 years may receive Fluad as part of routine clinical care during the influenza season.
High-Dose Quadrivalent Inactivated Influenza Vaccine (HD-IIV4)
Fluzone High-Dose Quadrivalent vaccine is an inactivated split virion influenza vaccine formulated to contain 240 mcg of HA total, with 60 mcg from each of the four recommended influenza strains in single-dose prefilled 0.7 mL syringes. Kaiser Permanente Northern California members =65 years may receive Fluzone High-Dose as part of routine clinical care during the influenza season.

Locations

Country Name City State
United States Kaiser Permanente Northern California (entire region) Oakland California

Sponsors (2)

Lead Sponsor Collaborator
Kaiser Permanente Seqirus

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Hospitalization for cardiovascular events KPNC members =65 years who receive Fluad or Fluzone High-Dose will be retrospectively assessed for hospitalization for cardiovascular events. This outcome will be assessed in single-season analyses (2023/24 and 2024/25 separately) and a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
Other PCR-confirmed influenza in subgroups with comorbidities KPNC members =65 years with comorbidities (e.g., cardiovascular and respiratory conditions, diabetes, obesity) who receive Fluad or Fluzone High-Dose will be retrospectively assessed for hospitalization for PCR-confirmed influenza. This outcome will be assessed in a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
Primary PCR-confirmed influenza KPNC members =65 years who receive Fluad or Fluzone High-Dose will be retrospectively assessed for the presence of PCR-confirmed influenza. This outcome will be assessed in single-season analyses (2023/24 and 2024/25 separately) and a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
Secondary Emergency department visit or hospitalization for PCR-confirmed influenza KPNC members =65 years who receive Fluad or Fluzone High-Dose will be retrospectively assessed for an emergency department visit or hospitalization for PCR-confirmed influenza. This outcome will be assessed in single-season analyses (2023/24 and 2024/25 separately) and a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
Secondary Hospitalization for PCR-confirmed influenza KPNC members =65 years who receive Fluad or Fluzone High-Dose will be retrospectively assessed for hospitalization for PCR-confirmed influenza. This outcome will be assessed in a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
Secondary Hospitalization for all-cause community-acquired pneumonia KPNC members =65 years who receive Fluad or Fluzone High-Dose will be retrospectively assessed for hospitalization for all-cause community-acquired pneumonia. This outcome will be assessed in single-season analyses (2023/24 and 2024/25 separately) and a pooled 2-seasons analysis (2023/24 and 2024/25 combined). =14 days after vaccination until date of outcome, death, loss-to-follow-up, or end of each season (estimated May 2024 or May 2025)
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