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Dexamethasone in community-acquired pneumonia.

Dexamethasone in community-acquired pneumonia. - Santeon-CAP study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43565
Enrollment
600
Registered
2011-12-05
Start date
2012-12-23
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Pneumonia respiratory tract infection

Interventions

Patients presenting with a community-acquired pneumonia, eligible for inclusion in the study, are treated with one bolus of dexamethasone 6 mg (1 tablet of 6 mg) on the emergency department and dexa

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 100 years with a community-acquired pneumonia which requires admission. Criteria to determine a community-acquired pneumonia: - Chest radiograph showing new opacities. In combination with two of the following findings: 0 Cough 0 Production of sputum 0 Temp >38,0 °C or 10.000 cells/mm3), leftward shift (>10%) or leucopenia (15 mg/l (three fold higher than the upper limit of normal)

Exclusion criteria

Exclusion criteria: - Immunocompromised patients: 0 Patients with a known congenital or acquired immunodeficiency. 0 Patients who received chemotherapy less than 6 weeks ago. 0 Patients who received corticosteroids in the last 6 weeks. 0 Patients who received immunosuppressive medication in the last 6 weeks (e.g. cyclosporin, cyclophosphamide, azathioprine). 0 Patients with COPD who are on systemic corticosteroids for COPD. - Patients who require ICU treatment. - Patients with tropical worm infection. - Patients with dexamethasone intolerance. - Pregnant and breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Length of hospital stay.

Secondary

MeasureTime frame
- 30-day mortality; - Admission to ICU after initial admission on the ward.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)