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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01686984
Other study ID # 2012/381
Secondary ID
Status Completed
Phase N/A
First received September 13, 2012
Last updated May 13, 2015
Start date September 2012
Est. completion date May 2015

Study information

Verified date May 2015
Source Region Skane
Contact n/a
Is FDA regulated No
Health authority Sweden: Swedish Medical Product Agency
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate how inspiratory flow pattern influences CO2 elimination in people without primary lung disease.

The hypothesis is that a long mean distribution time, caused by a long postinspiratory pause and high end-inspiratory flow, will promote CO2 exchange in the alveoli.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- No known primary lung disease

Exclusion Criteria:

- Primary lung disease

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Altered breath


Locations

Country Name City State
Sweden Division of Brain, Heart and Lungs, Neurosurgical Clinic, Skane University Hospital, Lund Lund Skane

Sponsors (1)

Lead Sponsor Collaborator
Region Skane

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Carbon dioxide elimination in a ventilator assisted breath. 30 minutes No
Secondary Blood CO2 concentration. 30 minutes No
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