Validation of the C-mo System - Cough Monitoring
Recruiting
N/A
Interventional Study
Cough
Asthma
Chronic Obstructive Pulmonary Disease
Gastro Esophageal Reflux
Idiopathic Pulmonary Fibrosis
Cough Frequency
Cough Severity
Coughing
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 2 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 300 (estimated)
- Sponsor
- Cough Monitoring Medical Solutions · Industry
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About This Trial
The goal of this clinical study is to validate C-mo System's ability to automatically detect and characterise cough, in patients over 2 years old with cough as a key or refractory symptom.
The main questions it aims to answer are:
1. Can C-mo System detect cough events? (automatic cough detection)
2. Can C-mo System characterise cough events? (calculation of cough intensity, identification of co…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients aged 2 years or older;
* Patients with symptoms/complaints of cough;
* Signed Informed Consent (age ≥ 18 years), signed Informed Consent from the parents/legal representative and the patient (16 and 17 years), or signed Informed Assent and Consent (5 years ≤ age ≤ 15 …
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