Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 1:22 AM
Ignite Modification Date: 2025-12-25 @ 1:22 AM
NCT ID: NCT00743093
Eligibility Criteria: Inclusion Criteria: * age 18 or older Exclusion Criteria: 1. History of acetaminophen ingestion on any of the four days preceding study enrollment 2. Measurable serum acetaminophen level at time of enrollment 3. Viral markers of Hepatitis B or C, or viral markers of Hepatitis A with an ALT level greater than ULN during screening laboratory testing 4. Serum ALT or AST level greater than ULN at Screening or Day 0 5. Total bilirubin level greater than ULN at Screening or Day 0 6. INR level greater than ULN at Screening 7. Alkaline phosphatase level greater than ULN at Screening 8. Platelet count less than 125 10\^9/L at Screening 9. Known cholelithiasis 10. Positive pregnancy test at Screening (female participants only) 11. History of consuming more than an average of 3 alcohol containing drinks daily over the preceding 2 weeks 12. History of consuming 3 or more alcohol containing drinks on any given day during the 2 weeks prior to study enrollment 13. New prescription medication started within the previous 30 days 14. Currently taking isoniazid 15. Currently taking warfarin 16. Currently adheres to a fasting type diet as determined by self report 17. Currently has anorexia nervosa as determined by self report 18. Participant is clinically intoxicated, psychiatrically impaired or unable to give informed consent for any reason 19. Known hypersensitivity or allergy to acetaminophen
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Study: NCT00743093
Study Brief:
Protocol Section: NCT00743093