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Continuous Infusion Piperacillin-tazobactam for the Treatment of Cystic Fibrosis

Piperacillin-tazobactam combination product · Phase 4

Registry ID
NCT01694069
Phase
Phase 4
Status
Terminated
Drug / intervention
Piperacillin-tazobactam combination product
Sponsor
West Virginia University
Start
2012-09
Enrollment
6
Locations
1

About this trial

Cystic fibrosis is an inherited disorder leading to chronic pulmonary inflammation and infection. A majority of people with cystic fibrosis have large quantities of bacteria residing in their lungs. One of the most common and harmful bacteria is called Pseudomonas aeruginosa. Patients with cystic fibrosis require frequent therapy with intravenous (I.V.) antibiotics to treat lung infections thought to be caused by Pseudomonas aeruginosa. One of the antibiotics frequently used to treat this bacteria is piperacillin-tazobactam. Piperacillin-tazobactam is thought to be the most effective when there is a constant level of drug in the body. The standard way to administer piperacillin-tazobactam is to give several grams 4 times each day as a 30 minute infusion. An alternative way to give piperacillin-tazobactam is by a continuous infusion; a continuous infusion will make it more likely that drug will remain at a constant level in the body. The objective of this study is to determine if administering piperacillin-tazobactam as a continuous infusion is more effective at treating people having a pulmonary exacerbation of cystic fibrosis than a standard 30 minute infusion, 4 times a day.

View NCT01694069 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT01694069 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.