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Local Antibiotic Delivery for Community Acquired Pneumonia - Pilot study (LANDCAP1)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511413-37-00
Enrollment
36
Registered
2024-06-18
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-10-01

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

Conditions

Community-acquired pneumonia

Brief summary

Proportion of patients with a drop in FEV1 of 20% or 300mL one hour following the first inhalation.

Detailed description

Proportion of patients with a drop in FEV1 of 20% or 300mL from baseline to day 4 or discharge, whichever comes first., CRP on day 4 higher than on any day from 1 to 3 including baseline., MAP ≤ 65 OR respiratory frequency > 25 OR pulse > 100 OR needing supplemental oxygen (1-4 of these fulfilled) on day 4., PCT on day 4 higher than baseline., Temperature ≥ 38.0 °C on day 4., Patient reported outcome measurements: Changes in Visual Analogue Scales for dyspnoea, cough and fatigue from baseline to day 4.

Interventions

DRUGSODIUM CHLORIDE

Sponsors

Gentofte Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Proportion of patients with a drop in FEV1 of 20% or 300mL one hour following the first inhalation.

Secondary

MeasureTime frame
Proportion of patients with a drop in FEV1 of 20% or 300mL from baseline to day 4 or discharge, whichever comes first., CRP on day 4 higher than on any day from 1 to 3 including baseline., MAP ≤ 65 OR respiratory frequency > 25 OR pulse > 100 OR needing supplemental oxygen (1-4 of these fulfilled) on day 4., PCT on day 4 higher than baseline., Temperature ≥ 38.0 °C on day 4., Patient reported outcome measurements: Changes in Visual Analogue Scales for dyspnoea, cough and fatigue from baseline to day 4.

Countries

Denmark

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026