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Completed

NCT Number: NCT01207245

Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis

Cystic fibrosis is the most common inherited life limiting condition which affects children. Patients with it develop lung infections which become difficult to clear, and damage the lungs. These are treated with antibiotics (such as tobramycin) into the vein (termed "intravenous antibiotics"). This has without doubt improved survival. However, all treatments have side effects. Tobramycin can cause kidney damage. The investigators have preliminary data that suggests that administering tobramycin in the morning may be safer for the kidneys than administering it in the evening.

The investigators plan to approach children and adults with cystic fibrosis whose doctors have decided to administer a course of intravenous tobramycin. The investigators will randomly allocate them to receive it at either 0800h or 2200h. The investigators will measure the rate at which the body eliminates tobramycin from the bloodstream, by measuring the amount of tobramycin in the blood stream after administering the antibiotic. For each patient the study will last for the duration of the course of antibiotics. This is decided by the doctor looking after the patient (rather than the researcher), and would typically be 14 days. The investigators will also measure substances in the blood and urine ("biomarkers") which are sensitive indicators of low levels of kidney injury. The investigators will monitor lung function and lung bacteria in both the groups to ensure that the patients in both groups improve by the same amount.

If the preliminary data are proved correct, this research will allow investigators to improve the safety profile of tobramycin, one of the most widely prescribed drugs in cystic fibrosis.

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Key information

Age range

5 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Nottingham University Hospitals NHS Trust

Nottingham, Nottinghamshire, NG7 2UH, United Kingdom

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of cystic fibrosis (CF) (defined as clinical features of CF plus a positive sweat test OR the presence of 2 genes known to be associated with CF disease)
  • Males or female 5 years and older
  • Treating doctor has decided to commence a course of tobramycin
  • Patient or parent / legal guardian able to give informed consent

Exclusion criteria

  • Previous episode of acute kidney injury
  • Solid organ transplantation
  • Evidence of impaired renal function (raised serum creatinine above the normal range for age)
  • Once daily aminoglycoside unsuitable because of hypersensitivity or previous high trough levels on once daily dosing.
  • Pregnancy

Treatment and study plan

Tobramycin time of administration

Other

Random allocation to time of day of administration of tobramycin

Primary outcomes

  1. Renal Elimination Rate Constant of Tobramycin

    Time frame: Days 1, 8 and 14

Secondary outcomes

  1. Weight

    Time frame: Day 1, 8, 14

  2. Pulmonary Function

    Time frame: Day 1, 8, 14

  3. Urinary Biomarkers

    Time frame: Days 1 and 14

    NAG, NGAL, IL-18, KIM1, Cystatin C

  4. Serum biomarkers

    Time frame: Days 1 & 14

    Serum creatinine Serum Cystatin C Estimated GFR

  5. Serum Electrolytes

    Time frame: Days 1 & 14

    Serum Potassium and Magnesium

Sponsors and collaborators

Lead sponsor

University of Nottingham

Other

Registry information

Official study title

Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis (CRITIC) A Randomized Pharmacokinetic Comparison of Tobramycin in Cystic Fibrosis

Acronym: CRITIC

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Sep 22, 2010
Registry last updated
Jun 23, 2015

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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