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Clinical Trials/TCTR20230510001
TCTR20230510001
Completed
Not Applicable

Safety and humoral immunogenicity of COVID-19 vaccine against SAR-CoV2 wild type and Omicron variant in patients with solid cancer

Faculty of Medicine, Chiang Mai University0 sites110 target enrollmentMay 10, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Solid cancerCOVID-19
Sponsor
Faculty of Medicine, Chiang Mai University
Enrollment
110
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 10, 2023
End Date
January 4, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. age 18 years or above
  • 2\. Has an appointment to receive vaccine against SAR\-CoV2
  • 3\. Confirmed diagnosis of solid tumor by pathology or imaging with any stages, treatments and responses after treatment that include complete remission disease within 1 year
  • 4\. Life expectancy is more than 6 months at the time receiving first dose of vaccine

Exclusion Criteria

  • 1\. Previously diagnosed COVID\-19 in the past 90 days
  • 2\. High\-risk epidemiology history within 14 days before enrolment e.g. close contact with index cases or visiting/ living in outbreak area
  • 3\. Receive blood products, blood components, or immunoglobulin within the past 90 days
  • 4\. Receive live attenuated vaccine in the past 28 days
  • 5\. Receive inactivated or subunit vaccines in the past 14 days
  • 6\. Women in lactation, pregnancy, or planned pregnancy during the study period
  • 7\. Known allergy to any vaccine component
  • 8\. Has signs and symptoms of active skin infection at injection site
  • 9\.Known history of HIV infection
  • 10\.Receive immunosuppressive drug

Outcomes

Primary Outcomes

Not specified

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