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OpenTrials
Completed

NCT Number: NCT00682942

How to Predict Lung Recruitment at the Bedside in Patients Affected by Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS)

The investigators aim to compare four different lung recruitment techniques (described in literature) to Computed tomography scan analysis.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Policlinico Hospital

Milan, 20100, Italy

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Sponsors and collaborators

Lead sponsor

Policlinico Hospital

Other

Registry information

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
May 23, 2008
Registry last updated
Dec 1, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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