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临床试验/NCT06252051
NCT06252051已完成4 期

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

Universitas Padjadjaran1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2021年1月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
76
试验地点
1
主要终点
Immunogenicity

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
40 Years 至 49 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Trivalent Vaccine

Experimental

干预措施: Trivalent Influenza Vaccine (Drug)

结局指标

主要结局

Immunogenicity

时间窗: 6 months

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

ILI Morbidity

时间窗: 6 months

Determined by the time from treatment to 6 months after

次要结局

  • Inflammatory interleukin measurements(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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