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Completed

NCT Number: NCT01400750

Comparison of 2 Treatment Regimens for Eradication of P Aeruginosa Infection in Children With Cystic Fibrosis

Treatment of new Pseudomonas aeruginosa (Pa) infection in cystic fibrosis (CF) can postpone chronic infection. Aim of the study: compare 2 Pa eradication regimens in children with new Pa infection.

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of pediatrics, CF center Uuiversity Hospital Leuven

Leuven, 3000, Belgium

About this study

Methods: CF children (0-18 years) with a new isolation of Pa from the airway were randomized to tobramycin inhalation solution (TOBI® 2x300 mg for 28 days) (TIS) or inhaled colistimethate sodium (Colistineb® 2x2 mill U daily) plus oral ciprofloxacin (30mg/kg/day) for 3 months (CC). The primary outcome was eradication at end of treatment. Secondary outcome parameters were time to Pa relapse, total and Pa specific IgG, FEV1, BMI and Pa status.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of CF (clinical signs consistent with CF and a sweat chloride > 60 mEq/l by quantitative pilocarpine iontophoresis and/or two CF causing mutations identified)
  • age 0 to 18 years old at time of inclusion
  • 'First' or 'new Pa infection' defined as 'first Pa isolation ever' or 'isolation of Pa from the airway (sputum, throat swab or BAL) after a Pa free interval of at least 6 months and documented with at least 3 negative cultures'.

Exclusion criteria

  • chronic Pa infection defined according to the Leeds criteria[17]
  • pulmonary exacerbation needing IV AB treatment at time of new Pa isolate
  • Pa isolation at time of CF diagnosis
  • patient already on an antipseudomonal antibiotic
  • interval between positive culture and start of treatment > 4 weeks.

Treatment and study plan

oral ciprofloxacin plus inhaled colistin

Drug

oral ciprofloxacin (30mg/kg/day divided in 2 doses) for 3 months (CC) plus inhaled colistimethate sodium(Colistineb® 2x2 mill U daily)

Other names: Ciproxin ® - ciprofloxacin, Colistineb ®

TOBI

Drug

tobramycin inhalation solution (TOBI® 2x300 mg) for 28 days

Other names: TOBI® - tobramycin inhalation solution (TIS)

Primary outcomes

  1. Pseudomonas aeruginosa eradication at the end of the treatment.

    Time frame: end of study drug treatment ie 3 months for CC and at 1 months for TIS

    sucessful eradication is defined as negative airway culture for P aeruginosa and end of study drug which is after 3 months for ciproxin-colistin (CC) and after 1 months for tobramycin for inhalation (TIS)

Secondary outcomes

  1. P aeruginosa eradication at 6 months after study entry

    Time frame: 6 months

    negative airway cultures for P aeruginosa up to 6 months after start of study drug

  2. time to new Pa positive culture (= relapse)

    Time frame: 1 year

    Time to first new P aeruginosa positive airway culture (expressed in months starting from end of study drug)

  3. change from baseline FEV1% pred, IgG z score, BMI z score was followed

    Time frame: 1 year

    Evolution of lung function (expressed as FEV1% pred), total IgG and nutritional status (expressed as BMI z score) from start of study up to 1 year

  4. Antibody titer for specific anti Pseudomonas antibodies

    Time frame: 1 year

    Pa antibodies (ELISA St Ag 1-17 )were measured at baseline and at 1 year follow-up

  5. P aeruginosa infection status

    Time frame: 1 year

    P aeruginosa infection status was reported as 'Free off', 'Intermittent' or 'Chronic' according to the Leeds criteria after 1 and 2 years.

    (ref Leeds criteria: Lee TW, Brownlee KG, Conway SP, et al. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros 2003;2(1):29-34)

  6. P aeruginosa infection status

    Time frame: 2 years

    P aeruginosa infection status was reported as 'Free off', 'Intermittent' or 'Chronic' according to the Leeds criteria after 1 and 2 years.

    (ref Leeds criteria: Lee TW, Brownlee KG, Conway SP, et al. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros 2003;2(1):29-34)

Sponsors and collaborators

Lead sponsor

Universitaire Ziekenhuizen KU Leuven

Other

Registry information

Official study title

Prospective Randomized Trial Comparing Oral Ciproxin Plus Inhaled Colistin With Tobramycin for Inhalation for Eradication of P Aeruginosa Infection in Children With Cystic Fibrosis.

Acronym: CCTOBI

Important dates

Study start
2001
Primary completion
2010
Study completion
2011
First posted
Jul 22, 2011
Registry last updated
Aug 4, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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