An Observational Study on the Impact of the 23-valent Pneumonia Vaccine on Lung Cancer Patients

ConditionLUNG CANCER
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital of Guangzhou Medical University

About this trial

To evaluate the impact of the 23-valent pneumonia vaccine on the incidence of pulmonary infection and survival in lung cancer patients, and to explore its preventive effect and safety in the lung cancer patients.

Eligibility criteria

Qualifiers

Male or female patients >=18 years of age;

Histological diagnosis of NSCLC, including both non-small cell lung cancer and small cell lung cancer, regardless of whether they are in the early, locally advanced stage or advanced stage, and regardless of whether they have received surgery, radiotherapy, chemotherapy or other treatments;

Never received pneumococcal vaccine

Disqualifiers

None

Trial design

Treatments tested in this trial

  • 23-valent pneumococcal vaccine

Treatment groups

500 Participants
are divided into 2 treatment groups

Locations

This trial has no locations