About this trial
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.
Eligibility criteria
Qualifiers
Male or female patients aged ≥ 18 years
Treatment with fosfomycin according to the (national) Summary of Product Characteristics (SmPC) of fosfomycin i.v.
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 infection, each as far as covered by the respective nationally relevant SmPC
Written informed consent of the participant (or person in charge in case of patients incapable of giving consent)
Disqualifiers
Previous documentation of the patient in the present study
Patients participating in an interventional clinical trial
Patients with known hypersensitivity to fosfomycin or any of the excipients
Terminally ill patients
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Infectopharm Arzneimittel GmbH
Lead sponsor
INPADS GmbH
Collaborator
Dr. Oestreich + Partner GmbH
Collaborator