Comparison of Different Mucoactive Agents for the Care of the Intubated Patient in a Surgical Trauma Intensive Care Unit
NCT ID: NCT00131521
Last Updated: 2009-06-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
260 participants
INTERVENTIONAL
2005-01-31
2007-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
DOUBLE
Interventions
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mucomyst
sodium chloride (saline)
Eligibility Criteria
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Inclusion Criteria
* Subjects must be eligible to start treatment within 24 hours of their initial intubation
Exclusion Criteria
* Hypersensitivity to acetylcysteine.
* Pregnancy
18 Years
ALL
No
Sponsors
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The University of Texas Health Science Center at San Antonio
OTHER
Principal Investigators
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John G. Myers, M.D.
Role: PRINCIPAL_INVESTIGATOR
University of Texas Health Science Center San Antonio
Locations
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Univesity Hospital
San Antonio, Texas, United States
Countries
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Other Identifiers
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034-1502-320
Identifier Type: -
Identifier Source: org_study_id
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