Effects of Therapeutic Doses of Acetaminophen in Moderate Drinkers

NCT00400621 | Completed Phase 4

• 1 other identifier: COMIRB 02-999
• Study Type: interventional
• Target: 150
• Locations: 0 countries
• Sites: N/A

Brief Summary

The study objective was to evaluate the safety of ten consecutive days of therapeutic acetaminophen dosing in moderate alcohol consumers. The main outcome was liver injury (measured by an increase in mean serum ALT or AST levels). Patients were randomly assigned to 10 days of acetaminophen or placebo. Blood tests were measured at baseline, day 4 and day 11 to look for injury. We hypothesized that there would be no difference in liver enzymes between the two groups.

Conditions

Moderate Alcohol Consumption (1-3 Drinks Per Day)

Keywords

acetaminophen; alcohol; liver injury

Outcome Measures

Primary Outcomes (1)

• mean change in serum ALT between treatment groups

Secondary Outcomes (3)

• proportion of patients that developed an abnormal ALT

• proportion of patients that developed hepatoxicity (ALT>1000 IU>L)

• proportion of patients that developed drug induced liver injury

Interventions

acetaminophen DRUG

Eligibility Criteria

• Age: 21 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Average baseline ethanol consumption of at least one alcoholic beverage per day before enrollment for the past two months. The estimate of ethanol intake was based on the average intake over seven days. For example, a person who ingested no alcohol on Sunday, Monday, Tuesday or Wednesday, two drinks on Thursday and four drinks on Friday and Saturday would be calculated as 10 drinks/7days = 1.4 drinks/day. The average alcoholic beverage contains 15 grams of alcohol(9).
• Average baseline ethanol consumption of no more than three alcoholic beverages (\> 45 grams of alcohol) per day, calculated as a weekly average over the preceding two months.
• At least one alcohol-containing drink within the last 48 hours

You may not qualify if:

• Subjects were excluded from the study at baseline if any of the following were evident at baseline:
• Serum acetaminophen level greater than 20 mcg/ml
• Serum AST or ALT levels greater than 50 IU/L
• If female, positive for b-HCG
• Clinically intoxicated, psychiatrically impaired or unable to give informed consent
• Known hypersensitivity to acetaminophen
• History of ingesting more than four grams of acetaminophen per day for any of the four days preceding study enrollment
• Alcoholic patients as defined by those who consume on average more than three alcoholic beverages daily
• Currently enrolled in another trial or had been enrolled in another trial in the preceding three months

Sponsors & Collaborators

• Denver Health and Hospital Authority: lead
• McNeil Consumer & Specialty Pharmaceuticals, a Division of McNeil-PPC, Inc.: collaborator

MeSH Terms

Interventions

Acetaminophen

Intervention Hierarchy (Ancestors)

Acetanilides; Anilides; Amides; Organic Chemicals; Aniline Compounds; Amines

Study Officials

• Kennon Heard, MD

  Rocky Mountain Poison Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 4
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: November 16, 2006
• First Posted: November 17, 2006
• Study Start: April 1, 2003
• Study Completion: September 1, 2003
• Last Updated: July 8, 2024

Record last verified: 2006-11