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NCT03966196 Clinical Trial

Validation and Characterization of Signal Decrease on an Oximeter in COPD (They Have Chronic Obstructive Pulmonary Disease) Patients During Deep Inhalation (

Copd Clinical Trial

— OXYMETRE  

Official title:
Validation and Characterization of Signal Decrease on an Oximeter in Chronic Obstructive Pulmonary Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03966196
Other study ID # 2018/25AVR/185
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 11, 2019
Est. completion date May 10, 2019

Study information
Verified date May 2019
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective is to verify that there is a decrease in the pulsed oxygen saturation with the digital sensor. That is, the drop in oxygen saturation in COPD patients during inhalation is real and not due to an artifact of the measuring tool, because oximeters need a quality pulsatile signal to properly measure oxygen saturation

Recruitment information / eligibility
Status Completed
Enrollment 12
Est. completion date May 10, 2019
Est. primary completion date May 10, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility healthy arm

Inclusion Criteria:

- Healthy adults volunteers are recruited from students with normal lung function.

Exclusion Criteria:

- abnormal lung function

COPD Arm

Inclusion Criteria:

- Adults with Chronic Obstructive pulmonary disease

Exclusion Criteria:

- cardiovascular disease

The subjects selected are selected on a voluntary basis among the patients coming to the pulmonary consultation. They have Chronic Obstructive Pulmonary Disease.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Measurements of oxygen saturation and finger pressure during deep inspiration
Measurements during deep inspiration of oxygen saturation with pulse oximeter and finger pressure with pressure cuff

Locations
Country Name City State
Belgium Cliniques universitaires Saint-Luc Brussels

Sponsors (1)
Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary drop in oxygen saturation during deep inspiration in COPD saturation is measured in percentage (SPO2) from the intervention to 3 minutes after the start of the intervention
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