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Not yet recruiting NCT07574866

A Retrospective Study on Clinical Characteristics and Outcomes of Patients With Pneumonia

Observational Pneumonia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Pneumonia. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Retrospective Analysis of Clinical Characteristics and Prognostic Factors in Hospitalized Pneumonia Patients from April 2023 to April 2026. Background: Pneumonia remains the leading cause of death from infectious diseases in adults worldwide, with an increasingly severe disease burden exacerbated by population aging and the frequent emergence of drug-resistant bacteria; in China, severe pneumonia accounts for a striking 13.58% to 20.05% of hospitalized cases. In recent years, shifts in the pathogen spectrum (e.g., COVID-19, influenza A) and patient demographic characteristics have posed new challenges for clinical management. However, existing studies mostly focus on single pathogens or specific populations (e.g., ICU patients), lacking systematic analyses of the full-disease course characteristics of general hospitalized pneumonia patients. Furthermore, in the post-pandemic era, the clinical phenotypes, treatment responses, and prognostic factors of pneumonia may have evolved, necessitating evidence-based support from real-world data. This study aims to conduct a retrospective analysis to clarify the epidemiological characteristics, etiological distribution, and prognostic factors influencing current hospitalized pneumonia patients, thereby providing a basis for optimizing diagnosis and treatment strategies.

Primary outcome measures

  • 28-day all-cause mortality rate [Time frame: 28 days after admission]
Secondary outcome measures (8)
  • Demographic characteristics [Time frame: 28 days after admission]
  • Comorbidities [Time frame: 28 days after admission]
  • Symptomatic manifestations [Time frame: 28 days after admission]
  • Laboratory tests [Time frame: 28 days after admission]
  • Imaging Examination [Time frame: 28 days after admission]
  • ICU Length of Stay [Time frame: 28 days after admission]
  • Duration of Mechanical Ventilation [Time frame: 28 days after admission]
  • Length of Hospital Stay [Time frame: 28 days after admission]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years old;
  • Meet the diagnostic criteria for pneumonia (acute onset + new infiltrates on imaging);
  • Have a positive result from pathogen testing;
  • Time from onset to admission ≤ 72 hours (to ensure being in the acute phase of the disease);
  • Sign a written informed consent form.

Inclusion criteria for the severe group:

A diagnosis of "severe pneumonia" can be made if one of the main criteria or ≥ 3 of the secondary criteria are met.

Main criteria:

① Tracheal intubation requiring mechanical ventilation

② Need for vasoactive drugs after active fluid resuscitation for septic shock

Secondary criteria:

  • Respiratory rate ≥ 30 breaths/min
  • PaO₂/FiO₂ ≤ 250 mm Hg
  • Multiple lobe infiltrates
  • Confusion and/or disorientation ⑤ Blood urea nitrogen ≥ 20 mg/dL

⑥ Leukopenia (WBC < 4×10⁹/L)

  • Thrombocytopenia (PLT < 100×10⁹/L)
  • Decreased body temperature (central body temperature < 36 ℃) ⑨ Hypotension requiring fluid resuscitation

Exclusion criteria

  • 1\) Patients with severely lacking medical records;

2\) Those whose main manifestations are other non-infectious diseases (such as pulmonary edema, lung cancer, pulmonary embolism, etc.); 3) Those whose main diagnosis is active pulmonary tuberculosis, non-infectious interstitial lung disease, etc.; 4) Patients considered not applicable by the researchers.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Fifth Affiliated Hospital of Guangzhou Medical University — Guangzhou

Identifiers

NCT: NCT07574866 · P-2026-003

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗