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Sponsored by: |
University Hospital, Ghent |
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Information provided by: | University Hospital, Ghent |
ClinicalTrials.gov Identifier: | NCT00458900 |
In the Intensive Care (IC)-unit moxifloxacin treatment is often started with intravenous administrations. As moxifloxacin is known to have a high oral bioavailability in healthy volunteers, patients are switched to oral or enteral therapy as soon as possible. However, no data on plasmalevels for moxifloxacin during such a switch-therapy in IC-patients are available. Therefore, this study aims to evaluate the moxifloxacin-plasmalevels and their inter-individual variability during IV to enteral switch therapy in IC-patients.
Condition | Intervention | Phase |
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Pneumonia |
Drug: IV and enteral administration of moxifloxacin |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study |
Official Title: | Pharmacokinetic Evaluation of Moxifloxacin IV to Enteral Switch Therapy in Intensive Care Patients |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Koen Boussery, Pharmacist, PhD | +32/(0)9/264.81.10 | koen.boussery@UGent.be |
Belgium | |
University Hospital Ghent | Recruiting |
Ghent, Belgium, 9000 | |
Contact: Koen Boussery, Pharmacist, PhD +32/(0)9/264.81.10 koen.boussery@UGent.be | |
Principal Investigator: Kirsten Colpaert, MD |
Principal Investigator: | Kirsten Colpaert, MD | University Hospital, Ghent |
Study ID Numbers: | 2007/071 |
Study First Received: | April 10, 2007 |
Last Updated: | December 19, 2007 |
ClinicalTrials.gov Identifier: | NCT00458900 |
Health Authority: | Belgium: Federal Agency for Medicinal Products and Health Products |
Respiratory Tract Infections Respiratory Tract Diseases Moxifloxacin Lung Diseases Pneumonia |
Anti-Infective Agents Therapeutic Uses Pharmacologic Actions |