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临床试验/NCT01207245
NCT01207245已完成4 期

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

University of Nottingham2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2011年5月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
18
试验地点
2
主要终点
Renal Elimination Rate Constant of Tobramycin

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
5 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Renal Elimination Rate Constant of Tobramycin

时间窗: Days 1, 8 and 14

次要结局

  • Weight(Day 1, 8, 14)
  • Pulmonary Function(Day 1, 8, 14)
  • Urinary Biomarkers(Days 1 and 14)
  • Serum biomarkers(Days 1 & 14)
  • Serum Electrolytes(Days 1 & 14)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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