EUCTR2014-002151-26-BE进行中（未招募）不适用
A Double Blind, Double Dummy, Randomized, Two Way Cross-Over Study To Compare The Effects Of Z7200 And Symbicort® Turbohaler On Functional Respiratory Imaging Parameters In Asthmatic Patients
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- Zambon Spa
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Male or female patient = 18 years old.
- •2. Written informed consent obtained.
- •3. Patient with a documented diagnosis of asthma according to the
- •Global Initiative for Asthma (GINA) guidelines
- •4. Patient with a co-operative attitude and ability to correctly use the DPI.
- •5. Female patient of childbearing potential who confirm that a reliable method of contraception was used at least 14 days before visit 1 and will continue to use a reliable method of contraception during the study, or post-menopausal women (at least 12 months of amenorrhea)
- •6. Patient must be stable and treated in accordance with the GINA guidelines.
- •7. Patient must be a non-smoker or ex-smoker who have stopped smoking at least 1 month prior to visit 1 and has a smoking history of < 10 pack years.
- •8. Patient must be able to understand and complete the protocol requirements, instructions, questionnaires and protocol-stated restrictions.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •1. Pregnant or lactating female.
- •2. Unstable patient who developed an asthma exacerbation in the 4 weeks before screening.
- •3. Patient with upper or lower airways infection in the 4 weeks before screening.
- •4. Patient unable to perform pulmonary function testing.
- •5. Patients unable to withdraw fixed combination or long acting bronchodilator inhalation products
- •6. Patient with an uncontrolled disease or any condition that might, in the judgement of the investigator, place the patient at undue risk or potentially compromise the results or interpretation of the study.
- •7. Patient with active lung cancer or any other chronic disease with poor prognosis and /or affecting patient status.
- •8. Patient with allergy, sensitivity or intolerance to study drugs and/ or study drug formulation ingredients.
- •9. Patient unlikely to comply with the protocol or unable to understand the nature, scope and possible consequences of the study.
- •10. Patient who received systemic corticosteroids within the last 4 weeks prior to visit
- •11. Patient who received any investigational new drug within the last 4 weeks prior to visit 1 and is participating in any clinical trial.
- •12. Patient with a history of alcohol or substance abuse that in the opinion of the investigator may be of clinical significance
- •13. Patient with diagnosis of Chronic Obstructive Pulmonary Disease (COPD).
- •14. Patients who has a lactose intolerance or history of allergy to milk proteins.
- •15. Patients treated with medications or herbal medicines that are strong cytochrome P450 3A4 (CYP3A4) inhibitors (e.g., ritonavir, indinavir, nelfinavir, saquinavir, atazanavir, ketoconazole, itraconazole, voriconazole, fluconazole, cyclosporine, mibefradil, nefazodone, clarithromycin, telithromycin, troleandromycin, norfloxacin, ciprofloxacin) or inducers (e.g. phenobarbital, phenytoin, barbiturates, carbamazepine, oxcarbazepine, rifabutin, rifampin, St John’s wort) within 2 weeks prior to Screening Visit and during the study.
研究者
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