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Efficacy and Safety of COVID-19 Vaccine in Cancer Patients

Malignant Solid Neoplasm Clinical Trial

Official title:
Efficacy and Safety of COVID-19 Vaccine in Cancer Patients

Clinical Trial Summary

This study gathers information about how a cancer patient responds to COVID-19 vaccine during cancer treatment compared to healthy individuals. The information gained may help determine how effective currently available COVID-19 vaccines are in cancer patients receiving chemotherapy and learn more regarding how long an immune response will last compared to healthy individuals.

Clinical Trial Description

PRIMARY OBJECTIVES: I. To determine the antibody response to COVID-19 vaccine after vaccination. II. To assess the adverse events of COVID-19 vaccines in cancer patients. III. To determine the incidence and severity of COVID-19 infection after the vaccination. OUTLINE: Patients undergo blood sample collection at baseline (prior to first COVID-19 vaccination), prior to second vaccination, 1, 6, and 12 months after the last vaccination. Patients receiving a booster vaccine will undergo blood collection prior to and 1-3 months after vaccination. Patients who receive the types of COVID-19 vaccines that do not require the second injection skip blood sample collection at this time point. This study will collect information regarding the type of COVID-19 vaccine received, date of vaccine injection, and any side effects associated with the COVID-19 vaccine that trial participant encountered. This study will also review the medical record for outcomes and information related to the blood testing. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04865133
Study type Observational
Source Mayo Clinic
Contact
Status Active, not recruiting
Phase
Start date March 31, 2021
Completion date December 31, 2024
View Details
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