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临床试验/NCT01311895
NCT01311895已完成3 期

Randomized Clinical Trial Comparing Two Protocols Using IV Hydromorphone

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 350 人开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
350
试验地点
1
主要终点
Number of Patients With Satisfactory Pain Management at 60 Minutes

研究概览

简要总结

The purpose of this study is to compare two opioid protocols ("H2O" and "1+1") for the treatment of acute severe pain in the emergency department. The investigators primary hypothesis is that the "H2O" protocol will be more efficacious than the "1+1" protocol in Emergency Department patients aged 21-64 years. The primary outcome is the proportion of patients in each arm who choose to forgo additional pain medication at 60 minutes.

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
Single (Participant)

入排标准

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

入选标准

  • Age greater than 21 years and less than 65 years: This is a study of non-elderly adult patients. In addition, patients aged 21 years and younger are automatically triaged to the Children's Emergency Department (ED).
  • Pain with onset within 7 days: Pain within seven days is the definition of acute pain that has been used in ED literature.
  • ED attending physician's judgment that patient's pain warrants intravenous (IV) opioids

排除标准

  • Use of other opioids or tramadol within past 24 hours: to avoid introducing assembly bias related to recent opioid use, since this may affect baseline levels of pain and need for analgesics.
  • Prior adverse reaction to opioids.
  • Chronic pain syndrome: frequently recurrent or daily pain for at least 3 months results in modulation of pain perception which is thought to be due to down-regulation of pain receptors. Examples of chronic pain syndromes include sickle cell anemia, osteoarthritis, fibromyalgia, and peripheral neuropathies.
  • Alcohol intoxication: the presence of alcohol intoxication as judged by the treating physician may alter pain perception.
  • Systolic Blood Pressure <90 mm Hg: Opioids can produce peripheral vasodilation that may result in orthostatic hypotension.
  • Oxygen saturation < 95% on room air: For this study, oxygen saturation must be 95% or above on room air in order to be enrolled.
  • Use of monoamine oxidase (MAO) inhibitors in past 30 days: MAO inhibitors have been reported to intensify the effects of at least one opioid drug causing anxiety, confusion and significant respiratory depression or coma.
  • CO2 measurement greater than 46: In accordance with standard protocol, three subsets of patients will have their CO2 measured using a handheld capnometer prior to enrollment in the study. If the CO2 measurement is greater than 46 then the patient will be excluded from the study. The 3 subsets are as follows:
  • All patients who have a history of chronic obstructive pulmonary disease (COPD)
  • All patients who report a history of asthma together with greater than a 20 pack-year smoking history
  • All patients reporting less than a 20 pack-year smoking history who are having an asthma exacerbation

研究组 & 干预措施

H2O

Experimental

2 mg IV hydromorphone administered over 2-3 minutes as initial dose

干预措施: H2O (Drug)

1+1

Experimental

1 mg IV hydromorphone followed by an additional 1 mg IV hydromorphone 15 minutes later if the patient answers "yes" to the following question: "Do you want more pain medication?"

干预措施: 1+1 (Drug)

结局指标

主要结局

Number of Patients With Satisfactory Pain Management at 60 Minutes

时间窗: 60 minutes

The primary outcome is the proportion of patients in each arm who choose to forgo additional pain medication at 60 minutes. This is defined as the number of patients who declined additional pain medication at 60 minutes.

次要结局

  • Number of Patients Who Reported no Pain or Mild Pain at 60 Minutes(60 minutes)
  • Mean Change in Pain Intensity From Baseline to 60 Minutes(60 minutes)

研究者

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

Andrew Chang, MD

Professor

Montefiore Medical Center

研究点 (1)

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