A study to evaluate ease of use and participants perception with breathe activated inhaler in comparison of pressurized meter dose inhaler in patients with Asthma or COPD and Healthy Volunteer.
Phase 4
Completed
- Conditions
- Health Condition 1: null- Patients with Asthma or COPD with no major other illness
- Registration Number
- CTRI/2015/08/006092
- Lead Sponsor
- Cipla Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 460
Inclusion Criteria
1. A written signed dated informed consent from all participants before study procedures.
2. Participants of both genders either healthy or confirmed diagnosis with Asthma (updated GINA 2015) aged between 5 and 80 years or confirmed diagnosis with COPD (updated GOLD 2015)aged between 40 to 80 years.
3. Patients using only pMDI device over past 3 months.
Exclusion Criteria
1. Current or past users of breath actuated inhaler
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method