Skip to content

Community-Acquired Pneumonia - Study on the Initial Treatment With Antibiotics of Lower Respiratory Tract Infections

Antibiotic Treatment of Community-acquired Pneumonia: a Prospective Comparison of Dutch Guideline Advices.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01660204
Acronym
CAP-START
Enrollment
2283
Registered
2012-08-08
Start date
2011-02-28
Completion date
2014-01-31
Last updated
2014-04-23

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

Conditions

Community-acquired Pneumonia

Keywords

pneumonia, anti-bacterial agents, (cost)efficacy

Brief summary

The purpose of this study is to compare the cost(effectiveness) of three existing antibiotic strategies for patients with community-acquired pneumonia admitted to the hospital, but not the ICU.

Interventions

OTHERPreferred empirical treatment

The investigators are using a cluster-randomized cross-over design for preferred empirical treatment. One of the 3 treatment arms is used as preferred empirical therapy during a period of 4 consecutive months, after which preferred treatment will rotate to 1 of the other 2 regimens. The order of change is randomised per hospital, thereby controlling for inter-hospital variables and minimizing seasonal influences.

Sponsors

ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients admitted to one of the participating hospitals needing treatment for CAP, not being admitted to the ICU are eligible for study inclusion. * Admission is defined as hospital stay for more than 24 hours.

Exclusion criteria

* Patients who are readmitted with CAP within 2 weeks after a previous episode are not eligible. * Patients with cystic fibrosis are not eligible.

Design outcomes

Primary

MeasureTime frameDescription
Day 90 Mortality90 days from admissionWe will assess all-cause mortality on day 90 from admission from the municipal personal records database

Secondary

MeasureTime frameDescription
Length of intravenous antibiotic treatmentParticipants will be followed for the duration of hospital stay, an expected average of 1 week
Length of hospital stayParticipants will be followed for the duration of hospital stay, an expected average of 1 week
TolerabilityParticipants will be followed for the duration of hospital stay, an expected average of 1 weekSide-effects and complications from antibiotic therapy are registered from clinical record
ComplicationsParticipants will be followed for the duration of hospital stay, an expected average of 1 weekComplications of pneumonia during admission are registered from clinical record.
Health care costs and non-health care costs28 days from admissionHealth care costs and non-health care costs are assessed using a short questionnaire 28 days from admission

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026