Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis (CRITIC)
Primary Purpose
Cystic Fibrosis
Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Tobramycin time of administration
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic fibrosis, Tobramycin, Pharmacokinetics, Toxicity
Eligibility Criteria
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
Sites / Locations
- Nottingham University Hospitals NHS Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Morning dose of tobramycin
Evening tobramycin
Arm Description
Administration of tobramycin once daily dose in the morning
Evening dose of tobramycin once daily
Outcomes
Primary Outcome Measures
Renal Elimination Rate Constant of Tobramycin
Secondary Outcome Measures
Weight
Pulmonary Function
Urinary Biomarkers
NAG, NGAL, IL-18, KIM1, Cystatin C
Serum biomarkers
Serum creatinine Serum Cystatin C Estimated GFR
Serum Electrolytes
Serum Potassium and Magnesium
Full Information
NCT ID
NCT01207245
First Posted
September 21, 2010
Last Updated
June 22, 2015
Sponsor
University of Nottingham
1. Study Identification
Unique Protocol Identification Number
NCT01207245
Brief Title
Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis
Acronym
CRITIC
Official Title
Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis (CRITIC) A Randomized Pharmacokinetic Comparison of Tobramycin in Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
June 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
Cystic fibrosis, Tobramycin, Pharmacokinetics, Toxicity
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Morning dose of tobramycin
Arm Type
Active Comparator
Arm Description
Administration of tobramycin once daily dose in the morning
Arm Title
Evening tobramycin
Arm Type
Active Comparator
Arm Description
Evening dose of tobramycin once daily
Intervention Type
Other
Intervention Name(s)
Tobramycin time of administration
Intervention Description
Random allocation to time of day of administration of tobramycin
Primary Outcome Measure Information:
Title
Renal Elimination Rate Constant of Tobramycin
Time Frame
Days 1, 8 and 14
Secondary Outcome Measure Information:
Title
Weight
Time Frame
Day 1, 8, 14
Title
Pulmonary Function
Time Frame
Day 1, 8, 14
Title
Urinary Biomarkers
Description
NAG, NGAL, IL-18, KIM1, Cystatin C
Time Frame
Days 1 and 14
Title
Serum biomarkers
Description
Serum creatinine Serum Cystatin C Estimated GFR
Time Frame
Days 1 & 14
Title
Serum Electrolytes
Description
Serum Potassium and Magnesium
Time Frame
Days 1 & 14
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan Smyth
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nottingham University Hospitals NHS Trust
City
Nottingham
State/Province
Nottinghamshire
ZIP/Postal Code
NG7 2UH
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
26282839
Citation
Prayle AP, Jain K, Touw DJ, Koch BC, Knox AJ, Watson A, Smyth AR. The pharmacokinetics and toxicity of morning vs. evening tobramycin dosing for pulmonary exacerbations of cystic fibrosis: A randomised comparison. J Cyst Fibros. 2016 Jul;15(4):510-7. doi: 10.1016/j.jcf.2015.07.012. Epub 2015 Aug 15.
Results Reference
derived
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Circadian Rhythm In Tobramycin Elimination In Cystic Fibrosis
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