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UnknownNCT05553379

Vivatmo proTM EU-study: FeNO Monitoring in Asthmatic Patients Responding to ICS Treatment

Clinical Study of the Vivatmo proTM for Fractional Exhaled Nitric Oxide (FeNO) Monitoring in Asthmatic Patients Responding to Inhaled Corticosteroid (ICS) Treatment

Status
Unknown
Phase
Study type
Observational
Enrollment
48 (actual)
Sponsor
Bosch Healthcare Solutions GmbH · Industry
Sex
All
Age
7 Years – 80 Years
Healthy volunteers

Summary

This is a multi-center study to evaluate fractional exhaled nitric oxide (FeNO) measured with the Vivatmo pro in adult and pediatric subjects.

Detailed description

Subjects will be screened, enrolled and tested at Study Visit #1 and then prescribed inhaled corticosteroid (ICS) treatment as per routine clinical care. Subjects will return for Study Visit #2 in two weeks and repeat fractional exhaled nitric oxide (FeNO) measured with the Vivatmo pro,

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTFeNO measurementFeNO measurement at each visit

Timeline

Start date
2022-03-15
Primary completion
2022-09-15
Completion
2022-10-15
First posted
2022-09-23
Last updated
2022-09-23

Locations

5 sites across 2 countries: Czechia, Germany

Regulatory

Source: ClinicalTrials.gov record NCT05553379. Inclusion in this directory is not an endorsement.

Vivatmo proTM EU-study: FeNO Monitoring in Asthmatic Patients Responding to ICS Treatment (NCT05553379) · Clinical Trials Directory