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Standard vs. Biofilm Susceptibility Testing in Cystic Fibrosis (CF)

Primary Purpose

Cystic Fibrosis, Chronic Bronchitis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
IV amikacin
PO azithromycin
IV ceftazidime
PO ciprofloxacin
IV meropenem
IV piperacillin-tazobactam
IV ticarcillin-clavulanate
IV tobramycin
Sponsored by
Seattle Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic fibrosis, Antibiotic susceptibility testing, Pseudomonas aeruginosa, Chronic bronchitis, Biofilms

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of CF based on the following: sweat chloride > 60 mEq/L (by quantitative pilocarpine iontophoresis), or genotype with 2 identifiable mutations consistent with CF; and one or more clinical features consistent with CF. Age ≥ 14 years (changed from ≥ 18 years by protocol amendment). Able to expectorate sputum at screening. History of persistent positivity for P. aeruginosa on respiratory culture (at least three positive oropharyngeal (OP), sputum and/or bronchoscopy cultures in the 24 months prior to screening). Able to reproducibly perform pulmonary function testing. Clinically stable at screening, with no evidence of pulmonary exacerbation. Written informed consent provided. Exclusion Criteria: Sputum culture negative for P. aeruginosa or density less than 10E5 CFU/gm at screening. Sputum culture positive for B. cepacia at screening. Presence of P. aeruginosa in sputum with off-scale resistance to all antibiotics by either method of susceptibility testing at screening. (changed from multiply-resistant P. aeruginosa by protocol amendment) History of B. cepacia positive respiratory culture within 24 months prior to screening. Hospitalization or treatment for a pulmonary exacerbation within 2 months prior to screening. Administration of parenteral anti-pseudomonal antibiotics within 2 months prior to screening. Treatment with oral or inhaled anti-pseudomonal antibiotics, or azithromycin or other macrolides within 14 days prior to screening. History of allergy (urticarial rash, diffuse erythroderma, serum sickness) to more than two groups of antibiotics (aminoglycosides, penicillins, cephalosporins, monobactams, macrolides, or quinolones) that are a therapeutic option. History of anaphylaxis or other life threatening complication to any antibiotic in the six groups that are a therapeutic option. History of abnormal renal function (serum creatinine > 1.5 x upper limit of normal) within one year of enrollment. History of abnormal liver function tests (> 2.5 x upper limit of normal) within one year of enrollment. Clinically documented hearing loss that precludes treatment with aminoglycosides. Post lung transplantation. Positive pregnancy test or female who is lactating or is not practicing an acceptable method of birth control. Presence of a condition or abnormality that in the opinion of an investigator would compromise the safety of the patient or the quality of the data. Administration of any investigational agent within 30 days prior to screening.

Sites / Locations

  • University of Iowa
  • Washington University St. Louis
  • University of Cincinnati
  • Ohio State University
  • University of Pittsburgh Medical Center
  • Baylor College of Medicine
  • Children's Hospital and Regional Medical Center
  • University of Washington Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Antibiotic regimen assignment based on biofilm susceptibility test results

Antibiotic regimen assignment based on conventional susceptibility test results

Outcomes

Primary Outcome Measures

Microbiological efficacy: Change in P. aeruginosa density

Secondary Outcome Measures

Clinical efficacy: Pre- to post-treatment change in FEV1
Safety: Adverse events, including new onset of acute pulmonary exacerbation and/or the need to change antibiotic therapy during the treatment period
Feasibility: Average costs and time per assay; rate of patient withdrawal because resistance patterns preclude randomization; self-reported technician satisfaction

Full Information

First Posted
September 8, 2005
Last Updated
March 12, 2008
Sponsor
Seattle Children's Hospital
Collaborators
Cystic Fibrosis Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00153634
Brief Title
Standard vs. Biofilm Susceptibility Testing in Cystic Fibrosis (CF)
Official Title
Standard vs. Biofilm Susceptibility Testing in CF
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Seattle Children's Hospital
Collaborators
Cystic Fibrosis Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This was a randomized multi-center clinical trial to compare the microbiological efficacy, clinical efficacy, and safety of using standard versus biofilm susceptibility testing of P. aeruginosa sputum isolates to guide antibiotic selection for treatment of airway infection in clinically stable patients with CF.
Detailed Description
Patients were screened to determine eligibility and to obtain a sputum culture. Eligible patients were randomized to either the standard or biofilm study arm. Antibiotic selection was performed centrally according to a standard algorithm using the susceptibility test results of the assigned study arm. On Day 0, patients were started on a 14-day course of two antibiotics as selected per protocol. Antibiotics were administered intravenously (IV) and/or orally. A follow-up phone call or visit occurred on Day 7. An end of treatment visit was conducted after completion of antibiotic therapy. A total of 39 patients were randomized. Many screened patients were ineligible for randomization based on microbiology results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Chronic Bronchitis
Keywords
Cystic fibrosis, Antibiotic susceptibility testing, Pseudomonas aeruginosa, Chronic bronchitis, Biofilms

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Antibiotic regimen assignment based on biofilm susceptibility test results
Arm Title
2
Arm Type
Active Comparator
Arm Description
Antibiotic regimen assignment based on conventional susceptibility test results
Intervention Type
Drug
Intervention Name(s)
IV amikacin
Intervention Description
5-7.5 mg/kg every 8 hrs or previous dose; start at previous recent stable dose then monitor serum levels and adjust dose, if needed, per standard clinical practice at the site
Intervention Type
Drug
Intervention Name(s)
PO azithromycin
Intervention Description
250 mg once daily
Intervention Type
Drug
Intervention Name(s)
IV ceftazidime
Intervention Description
50 mg/kg every 8 hours, up to 2 grams every 8 hours
Intervention Type
Drug
Intervention Name(s)
PO ciprofloxacin
Intervention Description
500 mg every 12 hours if weight <50 kg 750 mg every 12 hours if weight ≥50 kg
Intervention Type
Drug
Intervention Name(s)
IV meropenem
Intervention Description
40 mg/kg every 8 hours, up to 2 grams every 8 hours
Intervention Type
Drug
Intervention Name(s)
IV piperacillin-tazobactam
Intervention Description
100 mg/kg of piperacillin component every 6 hours, up to 3 grams every 6 hours; antibiotic combination formulated in a fixed ratio, thus dosing is described for first component only
Intervention Type
Drug
Intervention Name(s)
IV ticarcillin-clavulanate
Intervention Description
100 mg/kg of ticarcillin component every 6 hours, up to 3 grams every 6 hours; antibiotic combination formulated in a fixed ratio, thus dosing is described for first component only
Intervention Type
Drug
Intervention Name(s)
IV tobramycin
Intervention Description
2.5-3.3 mg/kg every 8 hrs or previous dose; start at previous recent stable dose then monitor serum levels and adjust dose, if needed, per standard clinical practice at the site
Primary Outcome Measure Information:
Title
Microbiological efficacy: Change in P. aeruginosa density
Time Frame
from enrollment (up to day -21) to end of treatment (day 12-14)
Secondary Outcome Measure Information:
Title
Clinical efficacy: Pre- to post-treatment change in FEV1
Time Frame
from initiation (day 0) to end of treatment (day 12-14)
Title
Safety: Adverse events, including new onset of acute pulmonary exacerbation and/or the need to change antibiotic therapy during the treatment period
Time Frame
from enrollment (up to day -21) to end of treatment (day 12-14)
Title
Feasibility: Average costs and time per assay; rate of patient withdrawal because resistance patterns preclude randomization; self-reported technician satisfaction
Time Frame
during active enrollment (March 2004-November 2007)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of CF based on the following: sweat chloride > 60 mEq/L (by quantitative pilocarpine iontophoresis), or genotype with 2 identifiable mutations consistent with CF; and one or more clinical features consistent with CF. Age ≥ 14 years (changed from ≥ 18 years by protocol amendment). Able to expectorate sputum at screening. History of persistent positivity for P. aeruginosa on respiratory culture (at least three positive oropharyngeal (OP), sputum and/or bronchoscopy cultures in the 24 months prior to screening). Able to reproducibly perform pulmonary function testing. Clinically stable at screening, with no evidence of pulmonary exacerbation. Written informed consent provided. Exclusion Criteria: Sputum culture negative for P. aeruginosa or density less than 10E5 CFU/gm at screening. Sputum culture positive for B. cepacia at screening. Presence of P. aeruginosa in sputum with off-scale resistance to all antibiotics by either method of susceptibility testing at screening. (changed from multiply-resistant P. aeruginosa by protocol amendment) History of B. cepacia positive respiratory culture within 24 months prior to screening. Hospitalization or treatment for a pulmonary exacerbation within 2 months prior to screening. Administration of parenteral anti-pseudomonal antibiotics within 2 months prior to screening. Treatment with oral or inhaled anti-pseudomonal antibiotics, or azithromycin or other macrolides within 14 days prior to screening. History of allergy (urticarial rash, diffuse erythroderma, serum sickness) to more than two groups of antibiotics (aminoglycosides, penicillins, cephalosporins, monobactams, macrolides, or quinolones) that are a therapeutic option. History of anaphylaxis or other life threatening complication to any antibiotic in the six groups that are a therapeutic option. History of abnormal renal function (serum creatinine > 1.5 x upper limit of normal) within one year of enrollment. History of abnormal liver function tests (> 2.5 x upper limit of normal) within one year of enrollment. Clinically documented hearing loss that precludes treatment with aminoglycosides. Post lung transplantation. Positive pregnancy test or female who is lactating or is not practicing an acceptable method of birth control. Presence of a condition or abnormality that in the opinion of an investigator would compromise the safety of the patient or the quality of the data. Administration of any investigational agent within 30 days prior to screening.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samuel M Moskowitz, MD
Organizational Affiliation
Seattle Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jane L Burns, MD
Organizational Affiliation
Children's Hospital and Regional Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Washington University St. Louis
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
University of Cincinnati
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45267-0557
Country
United States
Facility Name
Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Children's Hospital and Regional Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98105-0371
Country
United States
Facility Name
University of Washington Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15131149
Citation
Moskowitz SM, Foster JM, Emerson J, Burns JL. Clinically feasible biofilm susceptibility assay for isolates of Pseudomonas aeruginosa from patients with cystic fibrosis. J Clin Microbiol. 2004 May;42(5):1915-22. doi: 10.1128/JCM.42.5.1915-1922.2004.
Results Reference
background
PubMed Identifier
16188918
Citation
Moskowitz SM, Foster JM, Emerson JC, Gibson RL, Burns JL. Use of Pseudomonas biofilm susceptibilities to assign simulated antibiotic regimens for cystic fibrosis airway infection. J Antimicrob Chemother. 2005 Nov;56(5):879-86. doi: 10.1093/jac/dki338. Epub 2005 Sep 27.
Results Reference
background

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Standard vs. Biofilm Susceptibility Testing in Cystic Fibrosis (CF)

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