herpes zoster vaccine
BiologicalReceive the herpes zoster vaccine; Do not receive the herpes zoster vaccine
NCT Number: NCT07170059
To evaluate the impact of herpes zoster vaccine on the incidence of herpes zoster and survival in lung cancer patients, and to explore its preventive effect and safety.
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Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Receive the herpes zoster vaccine; Do not receive the herpes zoster vaccine
Time frame: 12 months
During the 12-month follow-up period, the incidence of herpes zoster in lung cancer patients was evaluated through regular clinical examinations, imaging tests, and laboratory tests.
Time frame: 24 months
The proportion of lung cancer patients who developed herpes zoster during the study period.
Time frame: 5 years
The survival rate of lung cancer patients within a specific time period (such as 1 year, 2 years, or 5 years).
Time frame: 5 years
Severity of herpes zoster and incidence of complications (e.g., postherpetic neuralgia)
Time frame: 5 years
Record the number of days of hospitalization for patients hospitalized due to herpes zoster
Time frame: 5 years
The proportion of patients hospitalized due to herpes zoster or other related complications.
Time frame: 5 years
The immune response (such as antibody levels) of patients after vaccination is evaluated through serological testing.
Time frame: 30 days
Observe whether patients who receive the herpes zoster vaccine experience adverse reactions after vaccination, such as fever, redness, swelling and pain at the injection site, headache, dizziness, etc.
The First Affiliated Hospital of Guangzhou Medical University
Other
An Observational Study on the Impact of Herpes Zoster Vaccine on the Incidence of Herpes Zoster and Survival in Lung Cancer Patients
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