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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06006845
Other study ID # pan-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2022
Est. completion date August 31, 2024

Study information

Verified date August 2023
Source The Seventh Affiliated Hospital of Sun Yat-sen University
Contact Xiaofen Pan, MD
Phone +8618124671750
Email panxf8@mail.sysu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to study the safety of initiation of antitumor therapy early after nucleic acid test turn negativity in tumor patients infected with COVID-19. The main questions aims to answer are: - Whether initiation of antitumor therapy early after nucleic acid test turn negativity in tumor patients infected with COVID-19 increases adverse events related to antitumor therapy. - Whether initiation of antitumor therapy early after nucleic acid test turn negativity in tumor patients infected with COVID-19 increases risk of re-infection of COVID-19. - How initiation of antitumor therapy early after nucleic acid test turn negativity in tumor patients infected with COVID-19 affects QoL of tumor patients Participants will be asked to answer the question about: - the severity and duration of COVID-19 symptoms - the date of diagnosis of COVID-19 - the date of negative nucleic acid test - the QoL of life before infection with COVID-19, during infection of COVID-19, after nucleic acid test negativity and receiving antitumor therapy


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date August 31, 2024
Est. primary completion date February 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Tumor patients diagnosed with COVID-19 infection at our center from December 1, 2022 to May 31. - COVID-19 was confirmed by antigen testing or nucleic acid testing. - Tumor was confirmed by pathology. - Patients received systemic antitumor therapy after infected with COVID-19. Exclusion Criteria: - COVID-19 was not confirmed by antigen testing or nucleic acid testing - Tumor was not confirmed by pathology - Patients did not receive systemic antitumor therapy - Patients died before receiving systemic antitumor therapy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Seventh Affiliated Hospital, Sun Yat-sen University Shenzhen Guangdong

Sponsors (1)

Lead Sponsor Collaborator
The Seventh Affiliated Hospital of Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of adverse events after antitumor therapy Incidence of adverse events after antitumor therapy, including hematologic toxicity,gastrointestinal adverse event, hepatobiliary adverse events, etc. 28 days after antitumor therapy
Primary Re-infection of COVID-19 Antigen testing or nucleic acid testing positive for COVID-19 28 days after antitumor therapy
Secondary Clinical manifestations of COVID-19 in tumor patients Symptoms and lab abnormality of COVID-19 in tumor patients Until nucleic acid testing turn negative
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