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临床试验/NCT01231139
NCT01231139已完成2 期

A Multi-centre Phase 2b Randomised Controlled Trial Investigating the Efficacy and Safety of Intravenous Paracetamol in Reducing Core Body Temperature After Traumatic Brain Injury

Dr. M.K. Saxena2 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
41
试验地点
2
主要终点
Core body temperature: bladder temperature probe

研究概览

简要总结

This primary aim is to investigate the effect of paracetamol in reducing body temperature in patients who have sustained traumatic brain injury. This study is also investigating the safety of paracetamol in this patient population.

详细描述

Traumatic head injury is a bruising of areas of the brain that occurs commonly as a result of a fall or a motor vehicle accident. Unfortunately, this is a common global occurrence and it occurs both in developing and developed countries. It causes death in nearly 1 in 3 of those who are most severely affected and a large proportion of those that survive have long-term physical or mental disability. Hence, traumatic head injury is a major global problem.

At present there are very few therapies that are known to be effective after a traumatic head injury. In particular the investigators are uncertain about whether modifying body temperature has any effect (good or bad) on the outcomes of patients. Although, this is practiced by some intensive care units around the world.

The investigators have searched extensively to look for any evidence that altering body temperature after traumatic head injury improves the outcome of patients (by reducing the amount of death or disability) and were unable to find any evidence at all. Some preliminary research in both animal experiments and clinical studies suggest that a raised temperature after forms of brain injury may in fact be harmful.

Therefore, at present the investigators believe that we do not really know what effect changing body temperature after head injury has on the outcome of patients.

The investigators are proposing to conduct a clinical study of patients who have had a severe head injury. The patients will be randomly allocated to 2 groups who will get either regular Paracetamol (dissolved in fluid) or a bottle of fluid without any Paracetamol. The 2 treatments will look identical and neither the patients nor the health care workers will know what treatment they are getting. Doing the study in this way will allow us to work out whether giving Paracetamol reduces the temperature of the body and whether there are any side effects that occur. If the study shows that Paracetamol can reduce body temperature safely in this setting then the investigators will work towards doing a larger study of treatments that reduce body temperature. The purpose of this larger study would be to see if the investigators can, not only reduce body temperature but also reduce amount of disability (physical and mental) as well as the death rate in traumatically brain injured patients.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Suspected paracetamol overdose or allergy to paracetamol
  • Confirmed or suspected pregnancy
  • Use of pharmacological or physical intervention that reduces body temperature in the 6-hour period prior to randomisation.
  • Clinician decision to institute any pharmacological or physical intervention that modifies body temperature
  • Body temperature at time of recruitment less that 36°C or greater than 38.9°C
  • History of chronic liver disease or chronic alcohol abuse
  • Suspected malnutrition: BMI < 18 kg/m2 or weight < 60 kg
  • BMI > 35 kg/m2
  • Renal failure with serum creatinine > 200
  • Haemodynamic instability defined as systolic blood pressure < 90 mmhg or requirement for noradrenaline or adrenaline exceeding 20mcg/minute
  • Use of hepatic enzyme inducers, except for phenytoin
  • Minor head injury: either normal CT head or not expected to be in intensive care for 72 hours
  • GCS = 3 with fixed dilated pupils
  • Moribund patient expected to die within 24 hours

研究组 & 干预措施

Paracetamol

Experimental

Paracetamol dissolved in 0.9% Sodium Chloride

干预措施: Paracetamol (Drug)

结局指标

主要结局

Core body temperature: bladder temperature probe

时间窗: 30 minutes after final dose of study drug has been administered

次要结局

  • Blood Pressure (systolic and mean arterial pressure) measured by intra-arterial pressure monitor(6 hourly during study treatment)
  • Liver function test(daily from first dose of study treatment to the 7th day)
  • serum Paracetamol levels (blood analysis) after a single dose of study drug and after final dose of study drug.(baseline, 30, 45, 90, 240 minutes after single dose. 240 minutes after final dose of study drug)
  • Temperature (bladder and tympanic)(Hourly from first study drug treatment until 4 hours after final study drug treatment)
  • The use of physical cooling interventions(hourly during the period of study intervention)
  • Intracranial pressure(6 hourly during the period of study intervention)
  • Incidence of cerebral hypoperfusion(During study intervention period)

研究者

发起方
Dr. M.K. Saxena
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr. M.K. Saxena

Intensive Care Physician

South East Sydney and Illawarra Area Health Service

研究点 (2)

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The Paracetamol AfteR Traumatic Brain InjurY Study | 临床试验