Target attainment of ciprofloxacin in patients admitted to a general ward: a prospective observational study
- Conditions
- Infections treated with ciprofloxacin, according to standard of care
- Registration Number
- NL-OMON25299
- Lead Sponsor
- Academic Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Receiving ciprofloxacin therapy intravenous (iv) or per os (po) as part of standard care
-Age ¡Ý 18 years
Exclusion Criteria
-Incapacitated patients, i.e. a minor or legally incompetent adult
-Treatment with ciprofloxacin is started elsewhere
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To investigate whether the current dosing regimen of ciprofloxacin, recommended by the SWAB guidelines and applied at the Academic Medical Center for patients with various degrees of renal function admitted at general wards, results in the target PK/PD index of AUC0-24/MIC ≥ 125.<br>
- Secondary Outcome Measures
Name Time Method