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NCT00568659 Clinical Trial

The Specific Lung Elastance in Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS) Patients in Supine and Prone Position

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
The Specific Lung Elastance in ALI/ARDS Patients in Supine and Prone Position

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00568659
Other study ID # 1111
Secondary ID
Status Completed
Phase N/A
First received December 5, 2007
Last updated April 27, 2015
Start date December 2007
Est. completion date January 2015

Study information
Verified date April 2015
Source Policlinico Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: National Monitoring Centre for Clinical Trials - Ministry of Health
Study type Interventional

Clinical Trial Summary

The investigators aim is to study the specific lung elastance in ALI/ARDS patients during invasive mechanical ventilation, in supine and prone position.

Description:

In sedated and paralyzed ALI/ARDS patients, we study and compare the specific lung elastance in supine and prone position during invasive mechanical ventilation.

Recruitment information / eligibility
Status Completed
Enrollment 15
Est. completion date January 2015
Est. primary completion date November 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ALI/ARDS patients during invasive mechanical ventilation

Exclusion Criteria:

- Haemodynamic failure, pneumothorax

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

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

Intervention

Procedure:
• specific elastance
The investigators study the specific lung elastance in ALI/ARDS patients in supine and prone position.

Locations
Country Name City State
Italy Policlinico Hospital Milano

Sponsors (1)
Lead Sponsor Collaborator
Policlinico Hospital

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Primary Specific elastance 5 minutes No
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