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临床试验/NCT01520792
NCT01520792已完成1 期

Paracétamol and Pharmacogenetic in Healthy Volunteers

University Hospital, Clermont-Ferrand2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2011年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Correlation between Pharmacogenetic profile and pain threshold

研究概览

简要总结

Recent works has emphasized that the mechanism of action of paracetamol analgesic depend on its metabolism in the body, since a breakdown product of paracetamol, the AM404 is now considered the analgesic metabolite of paracetamol suggesting as paracetamol may be a pro-drug.

Indeed, it has been shown that paracetamol may have a deleterious effect, especially in vulnerable populations (hepatic insufficiency, elderly). First results showed a very significant decrease in sulfatation and gluthatione and increased phase 1 metabolism of acetaminophen, which involves enzymes such as cytochrome P450.

Multifactorial causes, combining nutrition (depletion of sulfur amino acids), increased detoxification of toxic metabolites of paracetamol, stress or trauma are discussed to explain the results.

Clinical studies showed a great variability of pain assessment by patients and variability in the metabolic response of paracetamol. Genetic factors probably play a role remains largely unknown.

The review of the literature on genetic polymorphism shows the involvement of a number of enzymes that are well known, predominantly on the metabolism of acetaminophen liver, but without connection with its analgesic effect. This is a critical missing link in the understanding of the analgesic effect of paracetamol.

详细描述

Randomized, single-center, placebo-controlled, double-blind, cross-over in 100 healthy volunteers meeting the inclusion criteria and receiving 2g of paracetamol orally or placebo on two study periods separated by one week.

The evaluation criterion is the difference in areas under the curve of pain thresholds to thermal and mechanical stimulations test

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy volunteers
  • Aged between 18 and 30 years

排除标准

  • Subject without cons-indications of paracetamol

研究组 & 干预措施

Paracetamol

Experimental

干预措施: Paracetamol (drug) (Drug)

结局指标

主要结局

Correlation between Pharmacogenetic profile and pain threshold

时间窗: until 14 days before the administration

次要结局

  • Measures of thermal and mechanical pain thresholds(until 1 hour before the administration)
  • Determination of blood concentration of gluthatione(until 1 hour before administration)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (2)

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