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临床试验/NCT00743093
NCT00743093已完成4 期

Aminotransferase Trends During Prolonged Therapeutic Acetaminophen Dosing

Denver Health and Hospital Authority2 个研究点 分布在 1 个国家目标入组 398 人开始时间: 2008年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
398
试验地点
2
主要终点
The Proportion of Subjects Treated With Long-term Acetaminophen (4 g/Day) That Develops Persistent ALT Elevations.

研究概览

简要总结

The objective of this study is to monitor liver function tests (blood levels of an indicator of liver function) of healthy people taking the maximum labeled daily dose of acetaminophen compared to people taking placebo for 16 to 40 days. Those people that continue to have normal liver tests after 16 days will have completed their part of the study. People that develop abnormal liver function tests will continue taking acetaminophen or placebo, and have their liver tests monitored closely for up to an additional 24 days. This is to (1) make sure these tests return to normal and (2) determine when these tests return to normal while still taking acetaminophen or placebo. If at any time the liver tests indicate anything more than a minor increase, you would be immediately told to stop taking the study drug.

Secondary objective is to determine the proportion of subjects that have detectable acetaminophen-protein adducts after daily dosing.

详细描述

Acetaminophen use is common and many consumers take 4g/day for longer than 4 days. The use of 4g/day of acetaminophen for more than 4 days causes an asymptomatic ALT elevation in some people. This elevation most likely resolves while continuing treatment, but it is possible that some individuals may go on to develop clinical liver injury. By carefully following healthy subjects who are taking the maximal daily dose of acetaminophen, we can safely determine if the ALT elevation resolves or progresses to clinical liver injury. If a subject develops clinical liver injury we can intervene before irreversible injury occurs.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 18 or older

排除标准

  • History of acetaminophen ingestion on any of the four days preceding study enrollment
  • Measurable serum acetaminophen level at time of enrollment
  • Viral markers of Hepatitis B or C, or viral markers of Hepatitis A with an ALT level greater than ULN during screening laboratory testing
  • Serum ALT or AST level greater than ULN at Screening or Day 0
  • Total bilirubin level greater than ULN at Screening or Day 0
  • INR level greater than ULN at Screening
  • Alkaline phosphatase level greater than ULN at Screening
  • Platelet count less than 125 10^9/L at Screening
  • Known cholelithiasis
  • Positive pregnancy test at Screening (female participants only)
  • History of consuming more than an average of 3 alcohol containing drinks daily over the preceding 2 weeks
  • History of consuming 3 or more alcohol containing drinks on any given day during the 2 weeks prior to study enrollment
  • New prescription medication started within the previous 30 days
  • Currently taking isoniazid
  • Currently taking warfarin
  • Currently adheres to a fasting type diet as determined by self report
  • Currently has anorexia nervosa as determined by self report
  • Participant is clinically intoxicated, psychiatrically impaired or unable to give informed consent for any reason
  • Known hypersensitivity or allergy to acetaminophen

研究组 & 干预措施

acetaminophen

Experimental

acetaminophen, 4 grams/day (1 gram every 4 hours for 4 doses)

干预措施: acetaminophen (Drug)

placebo

Placebo Comparator

placebo for acetaminophen 4 grams/day (2 caplets every 4 hours for 4 doses)

干预措施: placebo (Drug)

结局指标

主要结局

The Proportion of Subjects Treated With Long-term Acetaminophen (4 g/Day) That Develops Persistent ALT Elevations.

时间窗: serial samples for 16-40 days

ALT was measured on Day 0 and 16 for all study participants. Subjects with an elevated ALT at Day 16 continued dosing with study drug and continued to have their ALT measured every three days until the ALT elevation resolved or until Day 40. Persistent ALT elevation was defined as any subject with an unresolved ALT elevation at study Day 40.

次要结局

  • The Proportion of Subjects With Detectable Serum Acetaminophen-cysteine Adduct (APAP-cys) Concentrations 1, 2, and 3 Days After Starting the Maximal Recommended Dosing of Acetaminophen (4 g/Day).(Days 1-3)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kennon Heard

Fellowship Director

Denver Health and Hospital Authority

研究点 (2)

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