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NCT Number: NCT06252051

Effectiveness of Trivalent Influenza Vaccine (TIV) in Type 2 Diabetes Mellitus (T2DM) Patients With and Without Complications of Chronic Kidney Disease (CKD)

This study assesses the effectiveness of the seasonal flu vaccine in individuals with Type 2 Diabetes Mellitus (T2DM) with and without Chronic Kidney Disease (CKD), as well as in healthy individuals. Additionally, the study investigates the dynamics of cytokines, specifically IL-2 and IL-6, in the three groups following influenza vaccination. The findings from these studies will contribute to our understanding of the safety and efficacy of the influenza vaccine in T2DM and T2DM-CKD, shedding light on inflammation changes and informing future research on mitigation strategies.

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Key information

About this study

The aim of this study is to assess the effectiveness of the influenza vaccine in the T2DM group, T2DM-CKD group, and healthy individuals without DM or CKD as a comparison. Patients with T2DM are characterized by low-grade inflammation, making them susceptible to infections, particularly influenza, leading to increased ICU admissions and mortality rates. Diabetes mellitus is also a major cause of declining kidney function, with complications known as diabetic kidney disease, ultimately progressing to chronic kidney disease, the most common cause of patients undergoing haemodialysis. The vulnerability to influenza infections prompts the recommendation for influenza vaccination in T2DM patients. Chronic kidney disease is a complication of diabetes that becomes intriguing to study regarding the effectiveness of the influenza vaccine in this group. Safety monitoring for all three groups is conducted for one month post-vaccination, assessing local symptoms such as redness at the injection site, pain, and systemic symptoms like fever, diarrhoea, weakness, or fatigue. Information related to influenza vaccine effectiveness is obtained by monitoring flu-like syndrome symptoms at months 1, 3, and 6. The researchers also examine interleukin levels, specifically IL-2 and IL-6, before and after vaccination for one month. This examination aims to understand the dynamic changes in both interleukins since IL-2 plays a role in protecting DM patients from influenza virus infections, particularly in preventing secondary infections like pneumonia.

The researcher's hypothesis is that T2DM-CKD patients will exhibit lower antibody responses compared to uncomplicated T2DM patients, and antibody titters against the influenza virus will decline after six months. This study will contribute valuable insights into the frequency of influenza vaccine administration in T2DM and T2DM-CKD groups, potentially reducing morbidity and mortality rates.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Group 1 (T2DM)

  • Individuals with Type 2 Diabetes Mellitus (T2DM)
  • Age range: 40-59 years

Group 2 (T2DM-CKD):

  • Individuals with Type 2 Diabetes Mellitus (T2DM)
  • Age range: 40-59 years
  • eGFR (ml/min/1.73 m2) >15
  • eGFR (ml/min/1.73 m2) <89
  • Proteinuria

Group 3 (Healthy Person) :

  • Individuals without Type 2 Diabetes Mellitus (T2DM)
  • Age range: 40-59 years

Exclusion criteria

  • Incomplete medical records
  • CKD Stage 5
  • Currently pregnant
  • Currently on long-term steroid use
  • Received influenza vaccine in the last year
  • Diagnosed with malignancy
  • Autoimmune disease
  • History of allergy to chicken eggs or vaccine constituents
  • High fever, seizures, or acute infection
  • History of COVID infection based on PCR testing with the last PCR result negative <14 days
  • History of COVID-19 vaccination <14 days from the last vaccine administration

Treatment and study plan

Trivalent Influenza Vaccine

Drug

We divided the participants into three groups: one comprising healthy individuals, another consisting of those with type 2 diabetes mellitus (T2DM), and the last group comprising individuals with T2DM and chronic kidney disease (CKD). All participants will receive a trivalent influenza vaccine, and various parameters will be observed.

Primary outcomes

  1. ILI Morbidity

    Time frame: 6 months

    Determined by the time from treatment to 6 months after

  2. Immunogenicity

    Time frame: 6 months

    Determine the changes in titers over time using the hemagglutination (HA) method at the 1st, 3rd, and 6th months after vaccination.

Secondary outcomes

  1. Inflammatory interleukin measurements

    Time frame: 6 months

    Inflammatory analysis will be performed in the 1st, 3rd, and 6th months.

Sponsors and collaborators

Lead sponsor

Universitas Padjadjaran

Other

Collaborators

  • Biofarma
  • Universiti Sains Malaysia

Registry information

Official study title

Effectiveness of Trivalent Influenza Vaccine (TIV) in Type 2 Diabetes Mellitus (T2DM) Patients With and Without Complications of Chronic Kidney Disease (CKD): A Clinical Observational Study on Antibody Titers and Dynamic Changes in IL-2 and IL-6 Cytokines

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Feb 9, 2024
Registry last updated
Feb 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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