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临床试验/JPRN-UMIN000026376
JPRN-UMIN000026376已完成4 期

ong-term Effect of Pulmonary Rehabilitation under Nintedanib treatment in Idiopathic Pulmonary Fibrosis - Long-term Effect of Pulmonary Rehabilitation under Nintedanib treatment in IPF

Central Japan Lung Study Grou0 个研究点目标入组 84 人开始时间: 2017年3月3日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
84

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
40years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with connective tissue disease, known neuromuscular disease or other orthopedic problem which may affect to exercise assessment, other disease requires exercise limitation 2)Patients who received pulmonary rehabilitation within 12 months 3)Patients with oral corticosteroids >15mg/day (prednisolone equivalent) or immunosuppressive agents within 3 months 4)Patients with pirfenidone within 3 months 5)Patients with unstable angina, a history of myocardial infarction or received percutaneous transluminal coronary angioplasty or coronary-artery bypass surgery within 1 month or a history of a cerebrovascular disease within 6 months. 6)Patients who requires antiarrhythmic therapy 7)Patients with serious pulmonary hypertension 8)ALT or AST > 2x upper limit of normal 9)Total bilirubin > 2x upper limit of normal 10)Creatinine clearance < 30mL/min 11)Patients who require fibrinolysis, full-dose therapeutic anticoagulation (e.g. vitamin K antagonists, direct thrombin inhibitors, heparin, hirudin) or high dose antiplatelet therapy. 12)Pregnant women and women of possibly pregnant. 13)Patients who cannot be evaluated by 6 minute walk test for any reason. 14)Other patients who are judged by the investigator as not adequate to participate in the study. 15)History of malignant disease within 3 years.

研究者

发起方
Central Japan Lung Study Grou

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