Trials / Terminated
TerminatedNCT02061852
Evaluation of the Safety of the Medical Device Simeox®
Prospective Trial for the Evaluation of Safety, Tolerability and Efficacy of the Medical Device Simeox ® Compared to Traditional Respiratory Physiotherapy Techniques for Airway Secretion Clearance
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- Physio-Assist · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether the medical device "simeox" is safe in the treatment of respiratory diseases, in comparison with traditional physiotherapy.
Conditions
- Broncho-degenerative Disease
- Chronic Obstructive Airway Disease
- Cystic Fibrosis
- Idiopathic Bronchiectasis
- Ciliary Dyskinesia
- Chronic Bronchitis
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Simeox | |
| PROCEDURE | Physiotherapy |
Timeline
- Start date
- 2014-07-01
- Primary completion
- 2015-09-01
- Completion
- 2015-09-01
- First posted
- 2014-02-13
- Last updated
- 2019-10-18
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT02061852. Inclusion in this directory is not an endorsement.