Hepatic Function During and Following Three Days of Acetaminophen Dosing in Alcoholics
NCT ID: NCT00402571
Last Updated: 2009-02-09
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
PHASE4
420 participants
INTERVENTIONAL
2002-01-31
2004-07-31
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
DOUBLE
Interventions
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acetaminophen
Eligibility Criteria
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Inclusion Criteria
1. 18 years or older
2. admitted to one of the two controlled access alcohol detoxification centers with a positive BAL at the time of admittance
3. signed a written informed consent form.
Patients were excluded from the study at baseline if any of the following were present:
1. serum acetaminophen level greater than 20 mcg/ml
2. serum AST or ALT levels greater than 200 IU/L
3. INR greater than 1.5
4. if female, positive for beta-subunit of chorionic gonadotropin
5. clinically intoxicated, psychiatrically impaired or unable to give informed consent
6. known hypersensitivity to acetaminophen
7. history of ingesting more than four grams of APAP per day for any of the four days preceding study enrollment
8. currently enrolled in another trial or had been enrolled in another trial in the preceding three months.
18 Years
ALL
Yes
Sponsors
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McNeil Consumer & Specialty Pharmaceuticals, a Division of McNeil-PPC, Inc.
INDUSTRY
Denver Health and Hospital Authority
OTHER
Principal Investigators
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Richard C Dart, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Denver Health/Rocky Mountain Poison & Drug Center
Locations
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Denver CARES
Denver, Colorado, United States
Recovery Centers of King County
Seattle, Washington, United States
Countries
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Other Identifiers
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COMIRB #00-715
Identifier Type: -
Identifier Source: org_study_id
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