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Clinical Trials/JPRN-UMIN000011462
JPRN-UMIN000011462
Recruiting
未知

The clinical study of the budesonide/formoterol combination drug additional dosage in the perioperative period in a lung cancer patient with COPD. - The clinical study of the budesonide/formoterol combination drug additional dosage in the perioperative period in a lung cancer patient with COPD.

Hamamatsu University School of Medicine0 sites40 target enrollmentAugust 12, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
on-small cell lung cancer patients with COPD.
Sponsor
Hamamatsu University School of Medicine
Enrollment
40
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 12, 2013
End Date
July 31, 2016
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\)Patient that there is ICS/LABA mixing medicine in pre\-administering within four weeks 2\)Patient where exacerbation of COPD was admitted within four weeks 3\)Patient that there is past of hypersensitivity in atropine, the kind edge material or tiotropium, budesonide or formoterol 4\)Patient who has chronic ailments of lungs, heart, kidney, liver, and blood, etc. 5\)Patient who has previous history of adrenal cortical insufficiency or accentuation syndrome 6\)Patient who has glaucoma 7\)Patient who has dysuria such as dysuria by enlarged prostate 8\)Case who judged doctor in charge targets and it is improper

Outcomes

Primary Outcomes

Not specified

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