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OpenTrials
Completed

NCT Number: NCT04905823

Effect of SARSCoV2 (COVID-19) Vaccination in Type 1 Diabetes (CoVaxT1D)

Given the high risk of severe SARS-CoV-2 infection, patients with T1D and T2D should represent a priority group to receive the SARS-CoV-2 vaccine. There are currently no studies on diabetic population response to mRNA COVID-19 vaccines. Therefore, in this observational cohort study, investigators will retrospectively analyze the safety and immunogenicity of the mRNA vaccines in eliciting both the humoral and cellular immune response in a subset of patients with T1D who already underwent blood sampling for measuring humoral response against SARSCoV2 for healthcare purposes and based on the clinical practice guidelines. Results will be compared with those obtained in non-diabetic individuals or in patients with non-autoimmune diabetes (T2D).

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

ASST FBF-Sacco P.O. Sacco

Milan, MI, 20157, Italy

About this study

Since the beginning of the COVID-19 pandemic in March 2020, more than 160 million people have suffered from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and more than 3 million deaths occurred. Currently, two vaccines using messenger RNA (mRNA) technology and lipid nanoparticle (LNP) delivery systems have been approved for emergency use by the Food and Drug Administration (FDA) and the European Medicines Agency (EMA): mRNA-1273, Moderna, and BNT162b2, Pfizer. In phase-3 clinical trials, two injections of these vaccines, spaced 21 and 28 days apart, showed efficacy higher than 90% in preventing symptomatic infections. The reported humoral immunity response with the mRNA vaccines was similar to that elicited by convalescent serum obtained from patients who recovered from Covid-19 infection. However, the T-cell mediated reaction to these vaccines remains to be fully elucidated. Diabetic patients are at higher risk of developing severe SARS-CoV-2 infection. In a large observational cohort study, the overall risks of fatal or critical care unit-treated COVID-19 were significantly elevated for patients with diabetes compared with the general population. While patients with Type 2 diabetes (T2D) are usually older and with a higher comorbidity index, the altered immune functions seem to play a major role in patients with Type 1 Diabetes (T1D). Altough an impaired immune response to vaccination was hypothesized in diabetic patients, no evidence has been provided. Given the high risk of severe SARS-CoV-2 infection, patients with T1D and T2D should represent a priority group to receive the COVID-19 vaccine. There are currently no studies on diabetic population response to mRNA COVID-19 vaccines. Therefore, in this observational cohort study, investigators will retrospectively analyze the safety and immunogenicity of the mRNA vaccines in eliciting both the humoral and cellular immune response in a subset of patients with T1D, T2D and in non-diabetic individuals who already underwent blood sampling for measuring humoral response against SARSCoV2 for healthcare purposes and based on the clinical practice guidelines.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

for patients with type 1 diabetes:

  • age >16
  • History of type 1 diabetes
  • previous blood test in search for SARSCoV2 antibodies
  • willingness to provide informed consent

Exclusion criteria

for patients with type 1 diabetes:

  • age <16 years
  • Systemic infections
  • Diabetic ketoacidosis in the past 6 weeks
  • COVID-19 diagnosis in the previous 6 months

Inclusion criteria

for non-diabetic subjects:

  • age >16
  • No previous history of diabetes
  • previous blood test in search for SARSCoV2 antibodies
  • willingness to provide informed consent

Exclusion criteria

for non-diabetic subjects:

  • age <16 years
  • Systemic infections
  • COVID-19 diagnosis in the previous 6 months

Inclusion criteria

for patients with type 2 diabetes:

  • age >16
  • History of type 2 diabetes but no evidence of autoantibodies
  • previous blood test in search for SARSCoV2 antibodies
  • willingness to provide informed consent

Exclusion criteria

for patients with type 2 diabetes:

  • age <16 years
  • Systemic infections
  • COVID-19 diagnosis in the previous 6 months

Treatment and study plan

Blood test

Diagnostic Test

assessment of humoral, immune cell response and glycemia

Primary outcomes

  1. Adverse events

    Time frame: change from baseline number at 2 months

    number of adverse events after SARSCov2 vaccination

Secondary outcomes

  1. Humoral response

    Time frame: change from baseline levels at 2 months

    Levels of antibodies detected against SARSCoV2

  2. Immune cell response

    Time frame: change from baseline levels at 2 months

    T cell response quantification

  3. Values of continuous glucose monitoring

    Time frame: change from baseline values at 2 months

    analysis of glycemic profile measured with continuous glucose monitoring

Sponsors and collaborators

Lead sponsor

Paolo Fiorina, MD

Other

Collaborators

  • ASST Fatebenefratelli Sacco

Registry information

Official study title

Effect of SARSCoV2 Vaccination in Type 1 Diabetes (CoVaxT1D)

Acronym: CoVaxT1D

Important dates

Study start
2021
Primary completion
2021
Study completion
2022
First posted
May 28, 2021
Registry last updated
May 10, 2023

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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