Scandinavian Cystic Fibrosis Azithromycin Study
Primary Purpose
Cystic Fibrosis
Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Study medication, azithromycin or placebo
Azithromycin or placebo tablets
Sponsored by

About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic Fibrosis, Pseudomonas aeruginosa, Azithromycin, Intermittent pulmonary infection
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Cystic Fibrosis based on genotype and/or positive sweat-test
- Written informed consent based on written and spoken information
- No chronic airway-infections with Gram-negative bacteria
- Fertile, sexually active women must use contraception (p-pills, IUD or other methods with a similar Pearl-index) when participating in the study
Exclusion Criteria:
- P. aeruginosa in airway secretions obtained less than 3 months prior to inclusion
- Chronic infection of the airways caused by Gram-negative bacteria (Burkholderia species, Achromobacter xylosoxidans, Pandorea apista or Stenotrophomonas maltophilia)
- Chronic infection of the airways caused by P. aeruginosa (chronic infection is defined by continuing growth of the microorganism for 6 months and/or an increase in specific, precipitating antibodies to a level of at least 2)
- Previous infection with a strain of P. aeruginosa resistant to ciprofloxacin or colistin
- Previous participation in a pseudomonas-vaccination-study
- Patients younger than 1 year
- Pregnant or lactating women, or sexually active women unwilling to use safe contraception (p-pills, IUD or method with similar Pearl-index) when participating in the study
- Severe insufficiency of the liver or kidneys as judged by the local investigator
Sites / Locations
- CF-centre Skejby, Skejby Sygehus, Brendstrupgaardsvej 100
- CF-centre Copenhagen, Rigshospitalet, Blegdamsvej 9
- CF-centre Bergen, Haukeland Universitetssykehus
- CF-centre Oslo, Ullevaal Universitetssykehus
- CF-centre Göteborg, Drottning Silvias barn- och ungdomssjukhus
- CF-centre Lund, Universitetssjukhuset i Lund
- CF-centre Stockholm, Karolinska Universitetssjukhuset, Huddinge
- CF-centre Uppsala, Akademiska Barnsjukhuset
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
A
B
C
Arm Description
Stratification group: Age under 8 years, no CF siblings at home.
Stratification group: Age >/= 8 years, no CF siblings at home.
Stratification group: Age >/= 8 years, CF siblings at home.
Outcomes
Primary Outcome Measures
Time to next airway-colonization (re-colonization) with Pseudomonas aeruginosa
Secondary Outcome Measures
Clinical condition of the patients (height, weight and lung function)
Bacteriological examination of Pseudomonas aeruginosa (phenotype, resistance)
Genotyping of Pseudomonas aeruginosa using Pulsed Field Gel Electrophoresis (re-infection caused by identical or new strain)
Specific, precipitating pseudomonas-antibodies (establishment of chronic infection)
Full Information
NCT ID
NCT00411736
First Posted
December 14, 2006
Last Updated
March 13, 2014
Sponsor
Rigshospitalet, Denmark
Collaborators
Cystic Fibrosis Foundation
1. Study Identification
Unique Protocol Identification Number
NCT00411736
Brief Title
Scandinavian Cystic Fibrosis Azithromycin Study
Official Title
Supplementary Oral Azithromycin in Treatment of Intermittent Pseudomonas Aeruginosa Colonization in CF-patients With Inhaled Colistin and Oral Ciprofloxacin; Postponing Next Isolate of Pseudomonas and Prevention of Chronic Infection. A Prospective, Double-blinded, Placebo-controlled Scandinavian Multi-centre Study.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
March 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
Cystic Fibrosis Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In patients with Cystic Fibrosis, recurrent airway infection caused by Pseudomonas aeruginosa ultimately leads to chronic airway infection. The purpose of this study is to determine whether supplementary low-dose azithromycin to standard inhaled colistin and oral ciprofloxacin in the treatment of intermittent pseudomonas airway-infection can postpone the next episode of intermittent pseudomonas airway-infection and prevent development of chronic airway-infection.
Detailed Description
Cystic Fibrosis is the most common genetic, inherited, deadly disease in caucasians. The disease is characterized by recurrent airway-infections caused by Pseudomonas aeruginosa, ultimately leading to chronic airway-infection, which is the main cause of the increased morbidity and mortality seen in this disease.
P. aeruginosa has the ability to change to mucoid phenotype - producing alginate and growing in biofilm, which protects the microorganisms from antibiotics and leukocytes. The change in phenotype is seen as chronic infection is established and eradication becomes impossible. Treatment with long-term, low-dose azithromycin in chronically infected CF-patients can improve the clinical condition of the patients. The exact mechanism for this is not known, but is possibly a combination of anti-inflammatory effects and the ability of azithromycin to inhibit alginate-production. Inhibition of biofilm-formation leaves the bacteria more susceptible to the actions of antibiotics and leukocytes.
Prior to establishment of chronic infection, recurrent, intermittent colonization of the airways with non-mucoid P. aeruginosa is seen. Intermittent infections can be treated using a combination of antibiotics, thereby postponing the next episode of airway-infection with P. aeruginosa.
The purpose of this study is to clarify wether supplementary azithromycin in the treatment of intermittent pseudomonas-infection in CF-patients can lead to further postponement of next pseudomonas-colonization and maybe prevent development of chronic infection. This is done in a randomised, double-blinded, placebo-controlled multicentre study.
2 treatments will be compared:
Inhaled colistin and oral ciprofloxacin in combination with oral azithromycin
Inhaled colistin and oral ciprofloxacin in combination with oral placebo.
The treatment will be given for 3 weeks, and the primary end-point is the time until next colonization with P. aeruginosa in the airways of the patients, comparing the 2 treatment-groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
Cystic Fibrosis, Pseudomonas aeruginosa, Azithromycin, Intermittent pulmonary infection
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
45 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Experimental
Arm Description
Stratification group: Age under 8 years, no CF siblings at home.
Arm Title
B
Arm Type
Experimental
Arm Description
Stratification group: Age >/= 8 years, no CF siblings at home.
Arm Title
C
Arm Type
Experimental
Arm Description
Stratification group: Age >/= 8 years, CF siblings at home.
Intervention Type
Drug
Intervention Name(s)
Study medication, azithromycin or placebo
Other Intervention Name(s)
Projectnumber HSA06-20/1
Intervention Description
Granulate for syrup in the group under 8 years, 40 mg/ml. Dose: 5 mg/kg/day in one daily dose.
Intervention Type
Drug
Intervention Name(s)
Azithromycin or placebo tablets
Other Intervention Name(s)
Project number HSA06-20/1
Intervention Description
Tablets of 250 mg, azithromycin or placebo. Dosage: 1 tablet every other day for participants with a weight less than 40 kg´s. 1 tablet every day for participants weighing 40 kg´s or more.
Primary Outcome Measure Information:
Title
Time to next airway-colonization (re-colonization) with Pseudomonas aeruginosa
Time Frame
up to 5 years
Secondary Outcome Measure Information:
Title
Clinical condition of the patients (height, weight and lung function)
Time Frame
up to 5 years
Title
Bacteriological examination of Pseudomonas aeruginosa (phenotype, resistance)
Time Frame
5 years
Title
Genotyping of Pseudomonas aeruginosa using Pulsed Field Gel Electrophoresis (re-infection caused by identical or new strain)
Time Frame
5 years
Title
Specific, precipitating pseudomonas-antibodies (establishment of chronic infection)
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of Cystic Fibrosis based on genotype and/or positive sweat-test
Written informed consent based on written and spoken information
No chronic airway-infections with Gram-negative bacteria
Fertile, sexually active women must use contraception (p-pills, IUD or other methods with a similar Pearl-index) when participating in the study
Exclusion Criteria:
P. aeruginosa in airway secretions obtained less than 3 months prior to inclusion
Chronic infection of the airways caused by Gram-negative bacteria (Burkholderia species, Achromobacter xylosoxidans, Pandorea apista or Stenotrophomonas maltophilia)
Chronic infection of the airways caused by P. aeruginosa (chronic infection is defined by continuing growth of the microorganism for 6 months and/or an increase in specific, precipitating antibodies to a level of at least 2)
Previous infection with a strain of P. aeruginosa resistant to ciprofloxacin or colistin
Previous participation in a pseudomonas-vaccination-study
Patients younger than 1 year
Pregnant or lactating women, or sexually active women unwilling to use safe contraception (p-pills, IUD or method with similar Pearl-index) when participating in the study
Severe insufficiency of the liver or kidneys as judged by the local investigator
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niels Hoiby, Prof.M.D.DSc
Organizational Affiliation
Department of Clinical Microbiology, Rigshospitalet
Official's Role
Principal Investigator
Facility Information:
Facility Name
CF-centre Skejby, Skejby Sygehus, Brendstrupgaardsvej 100
City
Aarhus N
ZIP/Postal Code
8200
Country
Denmark
Facility Name
CF-centre Copenhagen, Rigshospitalet, Blegdamsvej 9
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
CF-centre Bergen, Haukeland Universitetssykehus
City
Bergen
ZIP/Postal Code
5021
Country
Norway
Facility Name
CF-centre Oslo, Ullevaal Universitetssykehus
City
Oslo
ZIP/Postal Code
0407
Country
Norway
Facility Name
CF-centre Göteborg, Drottning Silvias barn- och ungdomssjukhus
City
Göteborg
ZIP/Postal Code
416 85
Country
Sweden
Facility Name
CF-centre Lund, Universitetssjukhuset i Lund
City
Lund
ZIP/Postal Code
221 85
Country
Sweden
Facility Name
CF-centre Stockholm, Karolinska Universitetssjukhuset, Huddinge
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden
Facility Name
CF-centre Uppsala, Akademiska Barnsjukhuset
City
Uppsala
ZIP/Postal Code
751 85
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
11106223
Citation
Doring G, Conway SP, Heijerman HG, Hodson ME, Hoiby N, Smyth A, Touw DJ. Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus. Eur Respir J. 2000 Oct;16(4):749-67. doi: 10.1034/j.1399-3003.2000.16d30.x.
Results Reference
background
PubMed Identifier
16023416
Citation
Hoiby N, Frederiksen B, Pressler T. Eradication of early Pseudomonas aeruginosa infection. J Cyst Fibros. 2005 Aug;4 Suppl 2:49-54. doi: 10.1016/j.jcf.2005.05.018.
Results Reference
background
PubMed Identifier
1679870
Citation
Valerius NH, Koch C, Hoiby N. Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment. Lancet. 1991 Sep 21;338(8769):725-6. doi: 10.1016/0140-6736(91)91446-2.
Results Reference
background
PubMed Identifier
12383667
Citation
Equi A, Balfour-Lynn IM, Bush A, Rosenthal M. Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial. Lancet. 2002 Sep 28;360(9338):978-84. doi: 10.1016/s0140-6736(02)11081-6.
Results Reference
background
PubMed Identifier
16127063
Citation
Gillis RJ, White KG, Choi KH, Wagner VE, Schweizer HP, Iglewski BH. Molecular basis of azithromycin-resistant Pseudomonas aeruginosa biofilms. Antimicrob Agents Chemother. 2005 Sep;49(9):3858-67. doi: 10.1128/AAC.49.9.3858-3867.2005.
Results Reference
background
PubMed Identifier
15752679
Citation
Hansen CR, Pressler T, Koch C, Hoiby N. Long-term azitromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study. J Cyst Fibros. 2005 Mar;4(1):35-40. doi: 10.1016/j.jcf.2004.09.001.
Results Reference
background
PubMed Identifier
9482305
Citation
Jaffe A, Francis J, Rosenthal M, Bush A. Long-term azithromycin may improve lung function in children with cystic fibrosis. Lancet. 1998 Feb 7;351(9100):420. doi: 10.1016/S0140-6736(05)78360-4. No abstract available.
Results Reference
background
PubMed Identifier
14519709
Citation
Saiman L, Marshall BC, Mayer-Hamblett N, Burns JL, Quittner AL, Cibene DA, Coquillette S, Fieberg AY, Accurso FJ, Campbell PW 3rd; Macrolide Study Group. Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial. JAMA. 2003 Oct 1;290(13):1749-56. doi: 10.1001/jama.290.13.1749.
Results Reference
background
PubMed Identifier
11867823
Citation
Wolter J, Seeney S, Bell S, Bowler S, Masel P, McCormack J. Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial. Thorax. 2002 Mar;57(3):212-6. doi: 10.1136/thorax.57.3.212.
Results Reference
background
PubMed Identifier
8585531
Citation
Kobayashi H. Biofilm disease: its clinical manifestation and therapeutic possibilities of macrolides. Am J Med. 1995 Dec 29;99(6A):26S-30S. doi: 10.1016/s0002-9343(99)80282-4.
Results Reference
background
Learn more about this trial
Scandinavian Cystic Fibrosis Azithromycin Study
We'll reach out to this number within 24 hrs