- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01239433
Pathophysiologic Changes in the Respiratory System During Therapeutic Interventions
Study Overview
Status
Conditions
Detailed Description
Airway pressures change during fiberoptic bronchoscopy and endotracheal suctioning. In this study such pressure changes are examined in a mechanical lung model and in a population of ICU patients on mechanical ventilation. A systematic recording of airway pressures, tidal volumes and blood gases are carried out during ordinary therapeutic procedures requested by the staff physician. No additional study interventions are carried out.
The aim of the project is to examine negative effects of pressure/volume changes.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Oslo, Norway, 0407
- Oslo University Hospital - Ulleval
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Patients in the Intensive Care Unit (ICU) on mechanical ventilation where daily endotracheal suctioning is performed to remove secretions.
Most of the patients have ARDS/ ALI.
Description
Inclusion Criteria:
- > 18 years of age
- on mechanical ventilation
- daily endotracheal suctioning performed
Exclusion Criteria:
- < 18 years of age
- non-invasive ventilation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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mechanically ventilated patients
ICU patients on mechanical ventilation.
Daily endotracheal suctioning performed to reduce secretions.
Data recorded during these therapeutic interventions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Intrabronchial airway pressure
Time Frame: 2013
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2013
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Espen R Nakstad, MD, Oslo University Hospital - Ulleval, Norway
- Study Director: Helge Opdahl, MD, PhD, Ullevaal University Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REK S-O, Ref 2010/1340, part B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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