Tiotropium Respimat Administration With and Without Aerochamber Disease (COPD)
NCT04999930 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2021-08-18
Summary
COPD patient on Tiotropium Respimart divided into two group, Group A given aerochamber and Group B without aerochamber enroll in the study for total 18 week .
Conditions
Interventions
- DEVICE
-
Aerochamber
efficacy and patients satisfaction
Sponsors & Collaborators
-
National University of Malaysia
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-01-10
- Primary Completion
- 2021-02-28
- Completion
- 2021-02-28
Countries
- Malaysia
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