LIPS-A: Lung Injury Prevention Study With Aspirin
Status: | Recruiting |
---|---|
Conditions: | Hospital, Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases, Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/2/2016 |
Start Date: | January 2012 |
End Date: | August 2016 |
This is a multi-center, phase, phase II double-blind, placebo-controled, randomized trial of
aspirin for the prevention of acute lung injury in patients identified as at risk for acute
lung injury.
aspirin for the prevention of acute lung injury in patients identified as at risk for acute
lung injury.
Inclusion Criteria:
- Adult patients (age > 18) admitted to the hospital through the emergency department
(ED)
- At high risk of developing ALI (Lung Injury Prediction Score-LIPS greater than or
equal to 4)
Exclusion Criteria:
- Anti-platelet therapy on admission or within 7 days prior to admission
- Presented to outside hospital ED > 12 hrs before arrival at site's facility
- Inability to obtain consent within 12 hours of hospital presentation
- Admitted for elective surgery
- Acute lung injury prior to randomization
- Receiving mechanical ventilation through a tracheostomy tube prior to current
hospital admission (patient who is ventilator dependent)
- Presence of bilateral pulmonary infiltrates on admission if he or she has a history
of bilateral pulmonary infiltrates (as evidenced by previous x-rays) that can
reasonably explain the current degree of pulmonary infiltrates present.
- Presentation due to pure heart failure and no other known risk factors for ALI.
- Allergy to aspirin or non steroidal anti inflammatory drugs (NSAID's)
- Bleeding disorder
- Suspected active bleeding or judged to be at high risk for bleeding
- Active peptic ulcer disease (within past 6 months)
- Severe chronic liver disease
- Inability to administer the study drug
- Expected hospital stay < 48 hours
- Admitted for comfort or hospice care
- Patient, surrogate or physician not committed to full support (Exception: a patient
will not be excluded if he/she would receive all supportive care except for attempts
at resuscitation from cardiac arrest)
- Not anticipated to survive > 48 hours
- Previously enrolled in this trial
- Enrolled in a concomitant intervention trial
- Pregnant or breastfeeding
We found this trial at
16
sites
University of Michigan The University of Michigan was founded in 1817 as one of the...
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Brigham and Women's Hosp Boston’s Brigham and Women’s Hospital (BWH) is an international leader in...
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Beth Israel Deaconess Medical Center Beth Israel Deaconess Medical Center (BIDMC) is one of the...
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Montefiore Medical Center As the academic medical center and University Hospital for Albert Einstein College...
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University of Illinois at Chicago A major research university in the heart of one of...
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Duke Univ Med Ctr As a world-class academic and health care system, Duke Medicine strives...
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Mayo Clinic Florida Thousands of people come to Mayo Clinic in Jacksonville, Fla., annually for...
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Mayo Clinic Rochester Mayo Clinic is a nonprofit worldwide leader in medical care, research and...
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Harborview Medical Center Harborview Medical Center is the only designated Level 1 adult and pediatric...
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