- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00682942
How to Predict Lung Recruitment at the Bedside in Patients Affected by Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS)
November 30, 2011 updated by: Davide Chiumello, Policlinico Hospital
The investigators aim to compare four different lung recruitment techniques (described in literature) to Computed tomography scan analysis.
Study Overview
Status
Completed
Conditions
Detailed Description
The investigators aim to compare four different lung recruitment techniques (described in literature) to Computed tomography scan analysis:
- stress index technique
- peep test
- recruitment technique used in the EXPRESS study
- recruitment technique used in the LOV study
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Milano, Italy, 20100
- Policlinico Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patients affected by acute lung injury/acute respiratory distress syndrome who are mechanically ventilated
Description
Inclusion Criteria:
- Clinical diagnosis of acute lung injury/ acute respiratory distress syndrome
- Mechanical ventilation
Exclusion Criteria:
- Clinical diagnosis of chronic obstructive pulmonary disease
- Clinical diagnosis of pneumothorax
- Haemodynamic instability
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: davide chiumello, md, Policlinico Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2008
Primary Completion (Actual)
June 1, 2011
Study Completion (Actual)
June 1, 2011
Study Registration Dates
First Submitted
May 21, 2008
First Submitted That Met QC Criteria
May 22, 2008
First Posted (Estimate)
May 23, 2008
Study Record Updates
Last Update Posted (Estimate)
December 1, 2011
Last Update Submitted That Met QC Criteria
November 30, 2011
Last Verified
November 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 16500
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.