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Japanese, multi-center, observational study for hospitalized patients with community-acquired, hospital-acquired, and ventilator-associated pneumonia

Japanese, multi-center, observational study for hospitalized patients with community-acquired, hospital-acquired, and ventilator-associated pneumonia - J-CAPTAIN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000042522
Enrollment
1500
Registered
2020-11-24
Start date
2020-11-24
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Community-acquired (CAP) including COVID-19, hospital-acquired (HAP), and ventilator-associated pneumonia (VAP)

Interventions

None listed

Sponsors

Nagoya University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The presence of a new infiltrate on a chest X-ray, or a computed tomography scan, plus at least one of the following criteria: 1) cough or purulent sputum, 2) pleuritic chest pain, 3) dyspnea, 4) fever or hypothermia (temperature >= 37.5 degrees or < 35 degrees), 5) white blood cell count >= 10,000 /mm3 or < 4,000 /mm3, 6) increase of CRP or PCT values above the upper limit of facility reference value and 7) hypoxemia (SpO2 < 90% or PaO2 < 60 Torr) or decline in oxygenation.

Exclusion criteria

Exclusion criteria: 1) Patients who do not receive initial empirical antibiotic treatment 2) Patients with obstructive pneumonia 3) Pneumonia occurred in other hospitals and patients who were transferred from their hospitals with a trend toward improvement 4) Patients whose pneumonia recurred within 3 days after the last day of antibiotic treatment of a preceding pneumonia episode 5) Patients who receive the treatment in outpatient clinics 6) Patients who are less than 20 years old

Design outcomes

Primary

MeasureTime frame
1) 30-day mortality, 90-day mortality and in-hospital mortality 2) Identified pathogens and drug resistance 3) Early and late treatment failure 4) Severe adverse events 5) Readmission within 90 days after discharge 6) Appropriateness of antibiotic treatment

Countries

Japan

Contacts

Public ContactYuichiro Shindo

Nagoya University Hospital Respiratory Medicine

yshindo@med.nagoya-u.ac.jp0527442167

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026