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Efficacy of Different Doses of Influenza Vaccine in Chronic Hemodialysis Patients (Enhance)

Primary Purpose

ESRD, Influenza Vaccine, Seroprotection

Status
Recruiting
Phase
Phase 4
Locations
Thailand
Study Type
Interventional
Intervention
Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated)
Sponsored by
Mahidol University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for ESRD focused on measuring ESRD, Influenza vaccine, double dose Influenza vaccine, double dose booster Influenza vaccine, Immune response

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥18 years
  • Received kidney replacement therapy with dialysis for more than 1 month.
  • Hemodialysis at least 3 times a week
  • (Kt/v) greater than 1.2
  • Never received an organ transplant.
  • Life expectancy of more than 1 year
  • Research participants or representatives are welcome to join the project by signing.

Exclusion Criteria:

  • History of any vaccinations in the 4 weeks prior to the study.
  • History of receiving influenza vaccine 6 months before entering this study.
  • History of allergy to flu vaccine or allergic to egg white
  • Fever or headache, muscle pain (influenza-like illness) 3 days before vaccination
  • Thrombocytopenia
  • On immunosuppressive drug (Prednisolone 15 mg daily or equivalent for two weeks in a row in the previous 3 months) or immunocompromised patient
  • Patient or family history of having had Guillain-Barre disease. (Guillain-Barre syndrome)
  • The research participant or his representative refuses or requests to withdraw.

Sites / Locations

  • Angsana PhuphuakratRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Active Comparator

Experimental

Experimental

Arm Label

้healthy subject with standard dose trivalent influenza vaccine

ESRD patient with standard dose trivalent influenza vaccine

ESRD patient with double dose trivalent influenza vaccine

ESRD patient with double dose - booster trivalent influenza vaccine

Arm Description

้healthy volunteer that received Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated) ( 0.5 ml : 15 mcg/strain)

ESRD patient that received Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated) ( 0.5 ml : 15 mcg/strain)

ESRD patient that received Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) total 1 ml ( 1 ml /(30 mcg/strain)

ESRD patient that received Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) ( 1 ml /(30 mcg/strain) and booster with Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) ( 1 ml /(30 mcg/strain) at next 6 months after first dose

Outcomes

Primary Outcome Measures

To compare proportion of seroprotection of different doses of influenza vaccine in hemodialysis patients at month 12
Patients will receive a blood test to check their immune response to influenza vaccine. (Hemagglutination inhibition assays and activation and/or exhaustion T cell markers, T cell subpopulation by flow cytometry) at month 12 after influenza vaccination.

Secondary Outcome Measures

To compare the prevention of influenza virus infection in different doses of influenza vaccination.
to compare incidence rate of influenza infection in different doses of influenza

Full Information

First Posted
September 4, 2021
Last Updated
November 1, 2021
Sponsor
Mahidol University
Collaborators
Bhumirajanagarindra Kidney Institute, Thailand, Ministry of Health, Thailand
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1. Study Identification

Unique Protocol Identification Number
NCT05070494
Brief Title
Efficacy of Different Doses of Influenza Vaccine in Chronic Hemodialysis Patients
Acronym
Enhance
Official Title
Efficacy of Different Doses of Influenza Vaccine in Chronic Hemodialysis Patients: Randomized Controlled Trial (Enhance Study)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
April 1, 2022 (Anticipated)
Study Completion Date
December 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mahidol University
Collaborators
Bhumirajanagarindra Kidney Institute, Thailand, Ministry of Health, Thailand

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
This study was a randomized controlled trial to investigate the immune response of influenza vaccines when doses were increased. and a second vaccination together with an increase in the amount of vaccine in patients with chronic kidney disease receiving hemodialysis
Detailed Description
Patients with chronic kidney disease undergoing dialysis will be examined by an internist. Collect the necessary basic information of patients who agree to participate in the treatment. Patients will be randomized to be divided into 3 groups: those who will receive an standard dose of influenza vaccine, those who will receive double standard dose of influenza vaccine (double-dose) and those who will receive double standard dose of influenza vaccine and Six months after the first dose of vaccination (double-booster-dose), 50 people per group. Non-dialysis volunteers will be invited to participate in the research. to be a control group of 25 people Patients with chronic kidney disease and volunteers will receive basic laboratory blood tests. Patients with chronic kidney disease and volunteers will be vaccinated against influenza. shoulder muscle area according to random groups The details of using Influvac vaccine of that year are produced by Abbott. Patients with chronic kidney disease and volunteers are asked about the potential side effects of vaccination. according to research guidelines both systemic side effects and injection site Each time receiving hemodialysis 3 times a week for 2 weeks after vaccination Patients with chronic kidney disease and volunteers were asked about the onset of symptoms of respiratory infection throughout the 12-month study period after vaccination. Patients will receive a blood test to check their immune response to influenza vaccine. (Hemagglutination inhibition assays and activation and/or exhaustion T cell markers, T cell subpopulation by flow cytometry) at 1, 6, 7 and 12 months after influenza vaccination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ESRD, Influenza Vaccine, Seroprotection
Keywords
ESRD, Influenza vaccine, double dose Influenza vaccine, double dose booster Influenza vaccine, Immune response

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
175 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
้healthy subject with standard dose trivalent influenza vaccine
Arm Type
Other
Arm Description
้healthy volunteer that received Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated) ( 0.5 ml : 15 mcg/strain)
Arm Title
ESRD patient with standard dose trivalent influenza vaccine
Arm Type
Active Comparator
Arm Description
ESRD patient that received Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated) ( 0.5 ml : 15 mcg/strain)
Arm Title
ESRD patient with double dose trivalent influenza vaccine
Arm Type
Experimental
Arm Description
ESRD patient that received Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) total 1 ml ( 1 ml /(30 mcg/strain)
Arm Title
ESRD patient with double dose - booster trivalent influenza vaccine
Arm Type
Experimental
Arm Description
ESRD patient that received Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) ( 1 ml /(30 mcg/strain) and booster with Egg-derived double dose trivalent influenza vaccine (surface antigen, inactivated) ( 1 ml /(30 mcg/strain) at next 6 months after first dose
Intervention Type
Biological
Intervention Name(s)
Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated)
Intervention Description
study of immunologic response to different dose and duration of Egg-derived standard dose trivalent influenza vaccine (surface antigen, inactivated)
Primary Outcome Measure Information:
Title
To compare proportion of seroprotection of different doses of influenza vaccine in hemodialysis patients at month 12
Description
Patients will receive a blood test to check their immune response to influenza vaccine. (Hemagglutination inhibition assays and activation and/or exhaustion T cell markers, T cell subpopulation by flow cytometry) at month 12 after influenza vaccination.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
To compare the prevention of influenza virus infection in different doses of influenza vaccination.
Description
to compare incidence rate of influenza infection in different doses of influenza
Time Frame
12 months of data collection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥18 years Received kidney replacement therapy with dialysis for more than 1 month. Hemodialysis at least 3 times a week (Kt/v) greater than 1.2 Never received an organ transplant. Life expectancy of more than 1 year Research participants or representatives are welcome to join the project by signing. Exclusion Criteria: History of any vaccinations in the 4 weeks prior to the study. History of receiving influenza vaccine 6 months before entering this study. History of allergy to flu vaccine or allergic to egg white Fever or headache, muscle pain (influenza-like illness) 3 days before vaccination Thrombocytopenia On immunosuppressive drug (Prednisolone 15 mg daily or equivalent for two weeks in a row in the previous 3 months) or immunocompromised patient Patient or family history of having had Guillain-Barre disease. (Guillain-Barre syndrome) The research participant or his representative refuses or requests to withdraw.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Angsana Phuphuakrat, MD, PhD
Phone
6622011581
Email
angsana.phu@mahidol.ac.th
Facility Information:
Facility Name
Angsana Phuphuakrat
City
Ratchathewi
State/Province
ฺBangkok
ZIP/Postal Code
10400
Country
Thailand
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angsana Phuphuakrat, MD, PhD
Phone
6622011581
Email
angsana.phu@mahidol.ac.th

12. IPD Sharing Statement

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Links:
URL
https://immunityageing.biomedcentral.com/articles/10.1186/1742-4933-9-19
Description
Related Info
URL
https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5916a2.htm
Description
Related Info

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Efficacy of Different Doses of Influenza Vaccine in Chronic Hemodialysis Patients

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