At What Time Therapeutic Plasma Concentrations of Paracetamol Are Achieved in Two Marketed Formulations
2012年3月8日 更新者:GlaxoSmithKline
A Randomised, Two Way Crossover Study to Determine the Time at Which Therapeutic Plasma Concentrations of Paracetamol Are Achieved in Two Marketed Formulations
This will be a single centre, open label, randomised, two-way crossover study in healthy volunteers under semi-fed conditions.
Two formulations of paracetamol, are being tested in this study to establish at what time point a therapeutic concentration of paracetamol in the blood is reached.
Subjects will attend a screening visit to check if they are eligible for study participation then within 15 days they will check-in to the unit for a stay of approximately 48 hours (hrs).
They will be given a single dose of one of the preparations on the first day and then the other preparation on the next day.
Regular blood samples will be taken along with other assessments for safety.
研究概览
研究类型
介入性
注册 (实际的)
12
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
N Ireland
-
Belfast、N Ireland、英国、BT9 6AD
- GSK Investigational Site
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 55年 (成人)
接受健康志愿者
是的
有资格学习的性别
男性
描述
Inclusion Criteria:
- Males in good general heatlh and Body Mass Index between 19-28 kg/m2
Exclusion Criteria:
Disease
- Current liver impairment, renal impairment, history of or active gastrointestinal ulcers, uncontrolled hypertension, haemophilia or other bleeding disorders.
- Current or recurrent disease, within 12 months of the screening, that could affect the action, absorption or disposition of the study formulations or clinical or laboratory assessments (e.g. hepatic disorders, renal insufficiency, congestive heart failure).
- Current or relevant previous history, within 12 months of the screening visit, of serious, severe or unstable physical or psychiatric illness, any medical disorder that may require treatment or make the subject unlikely to fully complete the study, or any condition that presents undue risk from the study treatments or procedures.
Medications
- Current or regular use at screening of any prescription, herbal or Over the Counter (OTC) medication including paracetamol, aspirin, metaclopramide, domperidone, cholestyramine, angiotensin -converting enzyme (ACE) inhibitors, acetazolamide, anticonvulsants, diuretics, methotrexate, non-steroidal anti-inflammatory drugs (NSAIDs) and oral hypoglycemics within the past 48 hrs and monoamine oxidase inhibitors, tricyclic antidepressants, beta blockers and anticoagulants such as warfarin and heparin within the past 2 weeks.
- Subjects who have taken any drug known to induce or inhibit hepatic drug metabolism in the 30 days prior to the screening visit (some examples of inducers: barbiturates, theophylline; inhibitors: cimetidine, erythromycin).
- Subjects for whom the use of any of the study drugs is contraindicated.
- Virology Screening Positive screening for serum Hepatitis B surface antigen, Hepatitis C antibodies or human immunodeficiency virus (HIV).
Drug Screen
- Positive urine screen for drugs of abuse at screening and/or Day-1.
- Positive alcohol breath test on Day-1.
Smoking
- Smoking more than five cigarettes a day.
- Prior (within 7 days of dosing on Day 1) or current use of any other nicotine containing products, other than cigarettes/pipes/cigars.
- Blood donation Has donated blood or plasma or any other blood product within 3 months of the screening visit. Subjects for whom participation in this study would result in having donated more than 1500 ml of blood within the previous 12 months.
Nutrition
- Is a vegetarian or is under a sodium restricted diet.
- Has consumed poppy seed containing foods within 3 days prior to the screening visit and admission on Day -1.
- Has consumed food and beverages containing grapefruit, Seville oranges or marmalade within 24 hrs prior to admission on Day -1.
- Has consumed caffeine containing drinks or food (e.g. tea, coffee, chocolate and cola) 24 hrs prior to admission on Day -1.
- Has consumed alcohol 36 hrs prior to admission on Day -1.
- Has undertaken any unusually strenuous physical activity 24 hrs prior to the screening visit or check-in on Day 1.
- Weight Weight below 50 kg.
- Haemoglobin Subjects with haemoglobin level below 12.0 gram /decilitre (dl).
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:Paracetamol formulation 1
Higher dose level of marketed paracetamol (compared to the other dosage arm)
|
formulation 1
|
|
其他:Paracetamol formulation 2
Lower paracetamol concentrations
|
Formulation 2
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Mean time to therapeutic levels of plasma concentration
大体时间:within a single day
|
within a single day
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Mean plasma concentrations
大体时间:within a single day
|
within a single day
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2009年6月1日
初级完成 (实际的)
2009年6月1日
研究完成 (实际的)
2009年6月1日
研究注册日期
首次提交
2011年6月23日
首先提交符合 QC 标准的
2012年3月8日
首次发布 (估计)
2012年3月13日
研究记录更新
最后更新发布 (估计)
2012年3月13日
上次提交的符合 QC 标准的更新
2012年3月8日
最后验证
2012年3月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.