JPRN-UMIN000022048
Completed
未知
The prospective study to evaluate the efficacy of the combination therapy of inhaled budesonide/formoterol fumarate, clarithromycin, and montelukast in AFO after allogeneic SCT - Chiba AFO-01 study
Department of Hematology, Chiba University Hospital0 sites85 target enrollmentApril 25, 2016
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Air flow obstruction after allogeneic SCT
- Sponsor
- Department of Hematology, Chiba University Hospital
- Enrollment
- 85
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\. Known history of intolerance or allergy to any triplet component. 2\. The patient who has past history of asthma and had attack within one year. 3\. The patient who has already been treated with the triplet combination. 4\. The patient who has active infection 5\. The patient who has mental disability requiring treatment 6\. The patient who has severe thromboembolism, including myocardial infarction, cerebral infarction, and cardiovascular complications. 7\. The patient who has uncontrollable diabetes mellitus and metabolic disease 8\. The patient who has other malignancy requiring anticancer treatment 9\. Pregnancy or nursing. 10\. At the time of enrollment as judged by the enrolling investigator would interfere with the subjects ability to comply with the study requirements
Outcomes
Primary Outcomes
Not specified
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