Clinical Trials Directory

Trials / Terminated

TerminatedNCT01694069

Continuous Infusion Piperacillin-tazobactam for the Treatment of Cystic Fibrosis

Continuous Infusion Piperacillin-Tazobactam for the Treatment of Pulmonary Exacerbations in Patients With Cystic Fibrosis

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
6 (actual)
Sponsor
West Virginia University · Academic / Other
Sex
All
Age
8 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

All patients will receive combination therapy to include piperacillin-tazobactam 400 mg/kg/day (based on piperacillin component, actual body weight) not to exceed 16 grams and tobramycin 12 mg/kg/day extended interval dosing (once daily). Patients randomized to the continuous infusion group will receive a one-time loading dose of 100 mg/kg over 30 minutes followed immediately by initiation of the continuous infusion. Other antibiotics with activity against Pseudomonas aeruginosa are not allowed. Patients may receive an antibiotic for treatment of Staphylococcus aureus if deemed appropriate. Other treatments for pulmonary exacerbation of cystic fibrosis will be left up to the control of the treating physician. Patients will receive a total of 14 days of therapy. If deemed appropriate, patients may be discharged to home where they will continue to receive blinded treatment via an infusion pump. Patients will be evaluated after completing their 14 day course of antibiotics (end of therapy).

Conditions

Interventions

TypeNameDescription
DRUGPiperacillin-tazobactam combination product400 mg/kg/day as either intermittent or continuous infusion

Timeline

Start date
2012-09-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2012-09-26
Last updated
2022-02-01
Results posted
2022-02-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01694069. Inclusion in this directory is not an endorsement.