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Moxifloxacin i.v. in the Treatment of Complicated Intra-Abdominal Infection (cIAI)

Information source: Bayer
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Secondary Peritonitis; Abscess, Intra-Abdominal

Intervention: Moxifloxacin (Avelox, BAY12-8039) (Drug)

Phase: N/A

Status: Completed

Sponsored by: Bayer

Official(s) and/or principal investigator(s):
Bayer Study Director, Study Director, Affiliation: Bayer


This study is a local, prospective, open-label, company-sponsored, non interventional, multi-center study. Patients documented must suffer from a cIAI and take at least one dose of Moxifloxacin infusion. The primary objective is to define the types of cIAI infections that require Moxifloxacin i. v. therapy in China.

Clinical Details

Official title: Clinical Effectiveness and Safety Study of Moxifloxacin i.v. in the Treatment of Complicated Intra-Abdominal Infection (cIAI)

Study design: Observational Model: Cohort, Time Perspective: Prospective

Primary outcome: Types of cIAI infections

Secondary outcome:

Cure rate

Clinical signs and symptoms

Duration until improvement and cure

Adverse event collection


Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.


Inclusion Criteria:

- Patients at least 18 years of age with a diagnosis of cIAI treated with Moxifloxacin

infusion with/without sequential tablet treatment can be included into the study. The local Moxifloxacin product information must be considered. Exclusion Criteria:

- Contraindications stated in the local Moxifloxacin product information. Warnings and

precautions, stated in the local Moxifloxacin product information must be considered as potential exclusion criteria.

Locations and Contacts

Many locations, China
Additional Information

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Starting date: December 2009
Last updated: June 20, 2013

Page last updated: August 23, 2015

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