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A randomized prospective controlled trial of long-acting muscarinic antagonist and long-acting be-ta2 agonist fixed dose combinations in patients with chronic obstructive pulmonary disease: Effects on quality of life and pulmonary function and preference

Not Applicable
Conditions
chronic obstructive pulmonary disease
Registration Number
JPRN-UMIN000041342
Lead Sponsor
Department of Respiratory Medicine and Allergology, Kindai University Nara Hospital
Brief Summary

o significant differences in CAT or mMRC were reported, and no significant difference in FEV1 was observed. Although FVC was higher after Ume/ Vil and Tio/ Olo administration, and MMF and V25 were higher after Gly/Ind administration, the differences reported were small. In the final comparative questionnaire survey, patients reported better actual feeling of being able to inhale following Gly/ Ind administration, although no significant differences in adverse events or other evaluations were reported.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
75
Inclusion Criteria

Not provided

Exclusion Criteria

Inability to inhale unassisted; inability to perform spirometry tests; pregnancy; severe comorbidities affecting quality of life, including malignancy, cardiac failure, renal failure, or severe liver dysfunction; and comorbidity of severe prostatic hypertrophy and closed-angle glaucoma.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Differences in preference, QoL, respiratory function, and adverse events among three medications
Secondary Outcome Measures
NameTimeMethod
The relationship between the medication selected as the first rank in the final comparative questionnaire and the background factors of the patients
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