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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2007-11-30
2008-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
2000 mg acetaminophen per day
acetaminophen
2 x 1000 mg doses per day
2
2000 mg cornstarch per day
cornstarch
2 x 1000 mg cornstarch per day
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
acetaminophen
2 x 1000 mg doses per day
cornstarch
2 x 1000 mg cornstarch per day
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Intake of enzyme-inducing drugs
* Prolonged fasting/eating disorders/gastroenteritis
* Intake of other over-the-counter or prescription analgesics
* Liver Disorders
* History of abuse treatment
17 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Toronto
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Geoff MacDonald, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Toronto
Nathan DeWall, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Kentucky
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Toronto
Toronto, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20619
Identifier Type: -
Identifier Source: org_study_id