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Local Antibiotic Delivery for Community Acquired Pneumonia (LANDCAP 2)

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511420-13-00
Enrollment
460
Registered
2024-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-11

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

Days alive and out of hospital at 14 days.

Detailed description

Days alive and out of hospital at 30 days., Days alive and out of hospital and without antibiotics at 30 days., Proportion of patient with antibiotic-related side-effects, Differences in gut microbiome diversity and composition in stool and oral samples on day 5 and on day 60., All-cause mortality at 30 days., Proportion of patients converted to guideline-based therapy according to algorithm as described in the section titled “Procedures, patient monitoring and data collection”., Proportion of patients readmitted, admitted to ICU or dead at 30 days., CRP on day 5, continuous and binary (higher than on any day from 1 to 4 including baseline)., MAP ≤ 65 OR respiratory frequency > 25 OR pulse > 100 OR needing supplemental oxygen (1-4 of these fulfilled) on day 5., PCT on day 5, continuous and binary (higher than on any day from 1 to 4 including baseline), Temperature ≥ 38.0 on day 5., Patient reported outcome measurements: Changes in Visual Analogue Scales for dyspnoea, cough, and fatigue from day 1 to day 5.

Interventions

DRUGSALINE
DRUGSODIUM CHLORIDE
DRUGPiperacillin/Tazobactam "Stada"
DRUGopløsning

Sponsors

Gentofte Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Days alive and out of hospital at 14 days.

Secondary

MeasureTime frame
Days alive and out of hospital at 30 days., Days alive and out of hospital and without antibiotics at 30 days., Proportion of patient with antibiotic-related side-effects, Differences in gut microbiome diversity and composition in stool and oral samples on day 5 and on day 60., All-cause mortality at 30 days., Proportion of patients converted to guideline-based therapy according to algorithm as described in the section titled “Procedures, patient monitoring and data collection”., Proportion of patients readmitted, admitted to ICU or dead at 30 days., CRP on day 5, continuous and binary (higher than on any day from 1 to 4 including baseline)., MAP ≤ 65 OR respiratory frequency > 25 OR pulse > 100 OR needing supplemental oxygen (1-4 of these fulfilled) on day 5., PCT on day 5, continuous and binary (higher than on any day from 1 to 4 including baseline), Temperature ≥ 38.0 on day 5., Patient reported outcome measurements: Changes in Visual Analogue Scales for dyspnoea, cough, and fatigue

Countries

Denmark

Outcome results

None listed

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