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Clinical Trials/JPRN-UMIN000026376
JPRN-UMIN000026376
Completed
Phase 4

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 sites84 target enrollmentMarch 3, 2017

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Idiopathic pulmonary fibrosis(IPF)
Sponsor
Central Japan Lung Study Grou
Enrollment
84
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 3, 2017
End Date
December 31, 2020
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Central Japan Lung Study Grou

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Not specified

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