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临床试验/NL-OMON35904
NL-OMON35904已完成不适用

The pharmacokinetic effect of clarithromycin on the AUC0-12h of linezolid in multidrug-resistant and extensively drug-resistant tuberculosis patients - LIN/CLA interaction study in MDR/XDR-TB patients

niversitair Medisch Centrum Groningen0 个研究点目标入组 7 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
7

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Age >=18 years old
  • - Signed informed consent
  • - Diagnosis of MDR-TB confirmed with standard microbiological criteria (culture-based, molecular or both)

排除标准

  • The criteria for exclusion are based on the contra indication as mentioned in the SPC texts of LIN and CLA.
  • - Hypersensitivity to: linezolid, clarithromycin, erythromycin, or any macrolide antibiotics, or any of the excipients of linezolid or clarithromycin.
  • - Concomitant use with astemizole, cisapride, ergotamine derivatives (dihydroergotamine, ergotamine), monoamine oxidase inhibitors (phenelzine, isocarboxazid, selegiline, or moclobemide), pimozide, or terfenadine.
  • - Pregnancy or breast-feeding.
  • - Hypokalemia
  • - Concomitant use of other P-glycoprotein inhibitors/inducers, e.g. amiodarone, verapamil, digoxin, tipranavir/ritonavir, lovastatin, tariquidar, itraconazole, dipyridamol, erythromycin, ritonavir, quinidine.
  • A pharmacist will check the co-medication of each patient for drug-drug interactions.

研究者

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