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Pulmonary inflammation during mechanical ventilation of patients with healthy lungs

Completed
Conditions
Mechanical ventilation, complications
Respiratory
Mechanical ventilation
Registration Number
ISRCTN77539853
Lead Sponsor
Academic Medical Centre (AMC) (The Netherlands)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria

1. Patients that are scheduled for surgical procedure of greater than 5 hours
2. Healthy pulmonary condition
3. 18 years of age
4. Informed consent

Exclusion Criteria

1. Sepsis or uncontrolled infection
2. Acute lung injury (ALI) or acute respiratory distress syndrome (ARDS)
3. Pneumonia
4. Steroid-use
5. Diagnosis of asthma
6. Pulmonary fibrosis
7. Current thrombo-embolism
8. On daily medication for chronic obstructive pulmonary disease (COPD)
9. Mechanical ventilation for greater than 48 hours in the month prior to surgery
10. Pneumonectomy/lebectomy
11. Participation in another trial
12. Previous randomisation in present trial

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Local levels of cytokines<br>2. Neutrophil influx<br>3. Activation of coagulation/inhibition of fibrinolysis<br>4. Ex vivo stimulation of alveolar macrophages<br>5. Systemic levels of biomarkers of lung injury
Secondary Outcome Measures
NameTimeMethod
o secondary outcome measures
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