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NCT00143468 Clinical Trial

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

ARDS Clinical Trial

Official title:
The Specific Elastance in Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS) Patients: Barotrauma and Volutrauma

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00143468
Other study ID # 1160
Secondary ID
Status Completed
Phase N/A
First received August 31, 2005
Last updated November 30, 2011
Start date March 2005
Est. completion date May 2008

Study information
Verified date November 2011
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 to study the specific elastance in ALI/ARDS patients during invasive mechanical ventilation.

Description:

In sedated and paralyzed ALI/ARDS patients, we studied the specific elastance and also, we compared the specific elastance to healthy subjects during invasive mechanical ventilation.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date May 2008
Est. primary completion date March 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years to 90 Years
Eligibility Inclusion Criteria:

- Stable ALI/ARDS patients during invasive mechanical ventilation

Exclusion Criteria:

- Hemodynamic 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

Intervention

Behavioral:
• mechanical ventilation
measurement of specific lung elastance during mechanical ventilation

Locations
Country Name City State
Italy Ospedale policlinico 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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