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CAPRIVI: Community Acquired Pneumonia: Treatment With Avelox® in Hospitalized Patients

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Bayer

Status

Completed

Conditions

Pneumonia

Treatments

Drug: Moxifloxacin (Avelox, BAY12-8039)

Study type

Observational

Funder types

Industry

Identifiers

NCT00987792
14522
AX0801 (Other Identifier)

Details and patient eligibility

About

The aim of this study is to obtain data from hospitalized Community Acquired Pneumonia (CAP) patients on the disease including disease severity, clinical signs and symptoms and measures used for diagnosis in daily routine practice as well as data on Avelox® including information on the use, effectiveness, treatment outcome, safety and tolerability.

As this is a non-interventional observational study, routine clinical practice is observed. The application of medications follows the normal routines and is decided by the treating physician under recognition of the package insert.

Enrollment

2,595 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult hospitalized patients with a diagnosis of CAP (based on local medical practice) and decision taken by the investigator to treat with moxifloxacin and to start treatment with intravenous administration. The local moxifloxacin product information must be considered.

Exclusion criteria

  • Contraindications stated in the local moxifloxacin product information; warnings and precautions must be considered.

Trial design

2,595 participants in 1 patient group

Group 1
Treatment:
Drug: Moxifloxacin (Avelox, BAY12-8039)

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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