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The Real World Effectiveness of Single Inhaler Triple Treatment through Assorted Respiratory Outcomes when Switched from Multiple Inhaler Triple Therapies (RESTART study)

Not Applicable
Recruiting
Conditions
Diseases of the respiratory system
Registration Number
KCT0007752
Lead Sponsor
Gyeongsang National University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
107
Inclusion Criteria

. Patients older than 40 years of age
-. Diagnosed with Chronic obstructive pulmonary disease
-. Agree with Participating Research
-. Treated by MITT(Multiple Inhaler Triple Treatment),(>=90days)

Exclusion Criteria

- a potentially pregnant patient
- Patients who are likely to die within 6 months or have poor health.
- Patients with unstable COPD with exacerbation within 4 weeks.
- Patients with other illnesses or mental illnesses.
- Patients who are hypersensitive to steroids and anti-choline, muscarinic drugs, and lactose/lactose proteins.
- Patients who use oral steroids for a long period of time (over 4 weeks) due to diseases other than COPD.
- Patients currently participating in interventional clinical research.

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change from baseline of CAT Score
Secondary Outcome Measures
NameTimeMethod
Change from baseline of FEV1;Over 2 point improved from baseline of CAT Score;Comparison of CAT Score improvements of more than 2 points for patients using the Elipta Device compared to patients who did not use the previous Elipta Device;Comparison of FEV1 improvements for patients using the Elipta Device compared to patients who did not use the previous Elipta Device; Clinically Important Deterioration (FEV1, Exacerbation, CAT);Comparison of FEV1 improvements for patients using the Elipta Device compared to patients who did not use the previous Elipta Device;Change from Baseline of mMRC;Over 1point improvement of baseline on mMRC;Change from baseline of TS-VAS;Exacerbation rate in 1 year
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