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NCT05827341 Clinical Trial

A Real-World Study of COVID-19 Infection in Patients With Malignant Lymphomas Participating in Clinical Trials

COVID-19 Clinical Trial

Official title:
A Real-World Study of COVID-19 Infection in Patients With Malignant Lymphomas Participating in Clinical Trials

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05827341
Other study ID # B2023-075-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2022
Est. completion date May 15, 2023

Study information
Verified date June 2023
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study focuses on the population of malignant lymphoma patients who are also in clinical research. Through a real world cross-sectional survey of infection and death risk during the COVID-19 pandemic in Guangzhou from December 2022 to January 2023, this study aims to clarify the risk, level and mortality of lymphoma patients infected with COVID-19 during their clinical research, and provide necessary research data for Chinese lymphoma patients during the COVID-19 pandemic,

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date May 15, 2023
Est. primary completion date January 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: (1) the diagnosis of lymphoma was confirmed by pathology according to World Health Organization (WHO)-criteria; (2) diagnosed with COVID-19 based on a positive polymerase chain reaction (PCR) test result for SARS-CoV-2 from oropharyngeal swabs, or on a positive detection of covid-19 antigen from nasopharyngeal swabs and typical clinical history; (3) participated in registered clinical trials and received anti-lymphoma treatment within four weeks before COVID-19 infection; (4) complete data on clinico-pathological characteristics, treatment approaches and follow-up were available. Exclusion Criteria: - Patients who could not provide detailed information about COVID-19 infection.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No intervention
No intervention needed

Locations
Country Name City State
China Department of Medical Oncology, Sun Yat-Sen University Cancer Center Guangzhou Guangdong

Sponsors (1)
Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The severity of COVID-19 The severity of COVID-19 infection in maligant lymphoma patients evaluated by investigators 2 months
Primary Hospital admission rate of COVID-19 infection The percentage of malignant lymphoma patients who were admitted into hospital 2 months
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