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Fosfomycin i.v. for Treatment of Severely Infected Patients — FORTRESS  

Sepsis Clinical Trial

Official title:
An International, Multicentre, Non-comparative, Non-interventional, Prospective Clinical Registry to Evaluate the Clinical Outcome and Safety of the Treatment of Severely Infected Patients With Fosfomycin i.v.

Clinical Trial Summary

The purpose of this European, multicentric, prospective, non-interventional study is to document and evaluate the efficacy and safety of the treatment of severely infected patients with intravenously administered fosfomycin, including patients with osteomyelitis, complicated urinary tract infection, nosocomial lower respiratory tract infection, bacterial meningitis/central nervous system infection, bacteraemia/sepsis, skin and soft tissue infection, endocarditis or other infections, each as far as covered by the respective nationally relevant SmPC.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Abscess
  • Bacteremia
  • Bacterial Infections
  • Bone Diseases
  • Bone Diseases, Infectious
  • Brain Abscess
  • Central Nervous System Bacterial Infections
  • Communicable Diseases
  • Encephalitis
  • Endocarditis
  • Endocarditis, Bacterial
  • Infections
  • Intraabdominal Infections
  • Meningitis
  • Meningitis, Bacterial
  • Osteomyelitis
  • Pneumonia
  • Pneumonia, Bacterial
  • Respiratory Tract Infections
  • Sepsis
  • Skin Diseases
  • Skin Diseases, Bacterial
  • Soft Tissue Infections
  • Urinary Tract Infections
Clinical Trial Details
NCT number NCT02979951
Study type Observational
Source Infectopharm Arzneimittel GmbH
Contact Thomas Borrmann, Dr.
Email Clinical.Trials@infectopharm.com
Status Recruiting
Phase
Start date December 2016
Completion date December 2030
View Details
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