Pulmonary Edema Clinical Trial
Official title:
The Effect of Nebulized Albuterol on Donor Oxygenation
Verified date | February 2018 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to test the effectiveness of albuterol versus placebo with the following specific aims: a) Treatment of brain dead organ donors with albuterol will reduce pulmonary edema, improve donor oxygenation, and increase the number of lungs available for transplantation, b) Developing a blood test to predict the development of primary graft dysfunction in lung transplant recipients, and c) treating brain dead organ donors with albuterol will decrease markers of primary graft dysfunction and lead to improved lung transplant recipient outcomes and to higher rates of lungs suitable for transplantation.
Status | Completed |
Enrollment | 506 |
Est. completion date | June 2011 |
Est. primary completion date | May 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 14 Years and older |
Eligibility |
Inclusion Criteria: - Brain death - Consent for lung donation and donor research - Release from coroner or medical examiner Exclusion Criteria - Age less than 14 years |
Country | Name | City | State |
---|---|---|---|
United States | California Transplant Donor Network | Oakland | California |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center | California Transplant Donor Network, University of California, San Francisco |
United States,
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Sundaresan S, Semenkovich J, Ochoa L, Richardson G, Trulock EP, Cooper JD, Patterson GA. Successful outcome of lung transplantation is not compromised by the use of marginal donor lungs. J Thorac Cardiovasc Surg. 1995 Jun;109(6):1075-9; discussion 1079-80. — View Citation
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* Note: There are 24 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Donor Oxygenation | The primary outcome was the change in oxygenation as measured by change in the PaO2/FiO2 ratio from study enrollment to organ procurement | Change from enrollment to organ procurement (about ~40h after enrollment) | |
Secondary | Number of Donor Lungs Used for Transplantation | Number of lungs procured and used for transplantation | 72 hours | |
Secondary | Lung Compliance | Static compliance of the respiratory system using plateau pressure (Pplat) measured at end-inspiration and calculated using the equation static compliance = tidal volume/(Pplat - PEEP) | baseline and at organ procurement (about ~40h after enrollment) | |
Secondary | Pulmonary Vascular Resistance | 72 hours | ||
Secondary | Chest X-ray Findings | Chest radiographs were scored using a radiographic score that scored each quadrant for extent of radiographic infiltrates on a scale of 0 to 4, then summed each quadrant for a total score from 0 (no infiltrates) to 16 (extensive infiltrates in all 4 radiographic quadrants). | change from enrollment to organ procurement (about ~40h after enrollment) |
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