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NCT00759590 Clinical Trial

Comparison of Two Methods to Estimate the Lung Recruitment

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
Comparisons of Two Methods to Estimate the Lung Recruitment

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00759590
Other study ID # 584
Secondary ID
Status Recruiting
Phase N/A
First received September 24, 2008
Last updated October 19, 2015
Start date September 2008

Study information
Verified date October 2015
Source Policlinico Hospital
Contact Davide Chiumello, MD
Phone 390255033237
Email chiumello@libero.it
Is FDA regulated No
Health authority Italy: Ministry of Health
Study type Observational

Clinical Trial Summary

In this study the investigators aim to compare two common methods to estimate the lung recruitment in ALI/ARDS patients.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- ALI/ARDS

Exclusion Criteria:

- Barotrauma

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

  • Acute Lung Injury
  • Acute Respiratory Distress Syndrome
  • Lung Injury
  • Respiratory Distress Syndrome, Adult
  • Respiratory Distress Syndrome, Newborn

Intervention

Procedure:
• CT scan and Pressure volume curve
CT scan

Locations
Country Name City State
Italy Policlinico Hospital Milano

Sponsors (1)
Lead Sponsor Collaborator
Policlinico Hospital

Country where clinical trial is conducted

Italy, 

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