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Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01207245
Acronym
CRITIC
Enrollment
18
Registered
2010-09-22
Start date
2011-05-31
Completion date
2012-06-30
Last updated
2015-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

Cystic fibrosis, Tobramycin, Pharmacokinetics, Toxicity

Brief summary

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.

Interventions

OTHERTobramycin time of administration

Random allocation to time of day of administration of tobramycin

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Renal Elimination Rate Constant of TobramycinDays 1, 8 and 14

Secondary

MeasureTime frameDescription
WeightDay 1, 8, 14
Pulmonary FunctionDay 1, 8, 14
Urinary BiomarkersDays 1 and 14NAG, NGAL, IL-18, KIM1, Cystatin C
Serum biomarkersDays 1 & 14Serum creatinine Serum Cystatin C Estimated GFR
Serum ElectrolytesDays 1 & 14Serum Potassium and Magnesium

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026