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Comparison of Two Methods to Estimate the Lung Recruitment

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2015 by Davide Chiumello, Policlinico Hospital.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00759590
First Posted: September 25, 2008
Last Update Posted: October 20, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Davide Chiumello, Policlinico Hospital
  Purpose
In this study the investigators aim to compare two common methods to estimate the lung recruitment in ALI/ARDS patients.

Condition Intervention
Acute Respiratory Distress Syndrome Acute Lung Injury Procedure: CT scan and Pressure volume curve

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparisons of Two Methods to Estimate the Lung Recruitment

Resource links provided by NLM:


Further study details as provided by Davide Chiumello, Policlinico Hospital:

Estimated Enrollment: 30
Study Start Date: September 2008
Primary Completion Date: March 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
1
ALI/ARDS patients
Procedure: CT scan and Pressure volume curve
CT scan

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
ALI/ARDS patients
Criteria

Inclusion Criteria:

  • ALI/ARDS

Exclusion Criteria:

  • Barotrauma
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00759590


Contacts
Contact: Davide Chiumello, MD 390255033237 chiumello@libero.it

Locations
Italy
Policlinico Hospital Recruiting
Milano, Italy
Contact: Davide Chiumello, MD    39025503237    chiumello@libero.it   
Principal Investigator: Davide Chiumello, MD         
Sponsors and Collaborators
Policlinico Hospital
Investigators
Study Chair: Davide Chiumello, MD Policlinico Hospital
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Davide Chiumello, MD, Policlinico Hospital
ClinicalTrials.gov Identifier: NCT00759590     History of Changes
Other Study ID Numbers: 584
First Submitted: September 24, 2008
First Posted: September 25, 2008
Last Update Posted: October 20, 2015
Last Verified: October 2015

Additional relevant MeSH terms:
Respiratory Distress Syndrome, Newborn
Respiratory Distress Syndrome, Adult
Acute Lung Injury
Lung Injury
Lung Diseases
Respiratory Tract Diseases
Respiration Disorders
Infant, Premature, Diseases
Infant, Newborn, Diseases
Thoracic Injuries
Wounds and Injuries