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Continuous Infusion Piperacillin-tazobactam for the Treatment of Cystic Fibrosis (PIPE-CF)

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West Virginia University

Status and phase

Terminated
Phase 4

Conditions

Cystic Fibrosis

Treatments

Drug: Piperacillin-tazobactam combination product

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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).

Enrollment

6 patients

Sex

All

Ages

8+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosis of cystic fibrosis
  2. 8 years of age or greater
  3. Chronic or intermittent infection with Pseudomonas aeruginosa as defined by the Leeds Criteria
  4. Pulmonary exacerbation as defined by Fuchs et al.

Exclusion criteria

  1. Admission for greater than 48 hours prior to enrollment
  2. Isolation of Burkholderia spp. in a respiratory tract culture in the prior 12 months
  3. Current treatment for allergic bronchopulmonary aspergillosis
  4. Pregnant or breast feeding
  5. History of solid organ transplantation
  6. Renal impairment at time of randomization (< 40 mL/min as calculated by the Cockcroft-Gault equation24 ¬for adults or the Schwartz equation45 for those < 18 years of age) or receipt of hemodialysis
  7. Allergy to study medication

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

6 participants in 2 patient groups

Intermittent Infusion piperacillin-tazobactam
Active Comparator group
Description:
Piperacillin-tazobactam administered at a dose of 400 mg/kg/day (maximum of 16 grams), divided in four equal doses, administered over 30 minutes, four times a day
Treatment:
Drug: Piperacillin-tazobactam combination product
Continuous infusion piperacillin-tazobactam
Experimental group
Description:
Piperacillin-tazobactam administered at a dose of 400 mg/kg/day (maximum of 16 grams) as a continuous infusion over 24 hours, once daily
Treatment:
Drug: Piperacillin-tazobactam combination product

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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