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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06252051
Other study ID # S3-202401.01
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 5, 2021
Est. completion date August 31, 2022

Study information

Verified date February 2024
Source Universitas Padjadjaran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date August 31, 2022
Est. primary completion date March 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 49 Years
Eligibility 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

Study Design


Intervention

Drug:
Trivalent Influenza Vaccine
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.

Locations

Country Name City State
Indonesia AMC Hospital Bandung West Java

Sponsors (3)

Lead Sponsor Collaborator
Universitas Padjadjaran Biofarma, Universiti Sains Malaysia

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary ILI Morbidity Determined by the time from treatment to 6 months after 6 months
Primary Immunogenicity Determine the changes in titers over time using the hemagglutination (HA) method at the 1st, 3rd, and 6th months after vaccination. 6 months
Secondary Inflammatory interleukin measurements Inflammatory analysis will be performed in the 1st, 3rd, and 6th months. 6 months
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