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Ventilation with lower tidal volumes as compared to traditional tidal volumes of patients not suffering from acute lung injury

Completed
Conditions
Mechanical ventilation, complications
Respiratory
Ventilation
Registration Number
ISRCTN82533884
Lead Sponsor
Academic Medical Centre (AMC) (Netherlands)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
200
Inclusion Criteria

Patients who are intubated and expected to receive mechanical ventilation for greater than 72 hours are eligible for the study if they do not suffer from Acute Lung Injury (ALI)/Acute Respiratory Distress Syndrom (ARDS), according to the American/European consensus criteria.

Exclusion Criteria

1. Greater than 36 hours after start of Mechnical Ventilation (MV)
2. Under 18
3. Participation in other trials
4. Pregnancy
5. Increased uncontrollable intracranial pressure
6. Severe chronic respiratory disease (daily medication)
7. Pneumonia
8. Use of corticosteroids (systemic or local) or other immunosuppressive agents
9. Pulmonary thrombo-embolism
10. After pneumonectomy or lobectomy
11. Previous randomisation in this study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Local inflammatory responses<br>2. Local Fibrin turnover<br>3. Systemic levels of biomarkers of lung injury
Secondary Outcome Measures
NameTimeMethod
ate ALI/ARDS.
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