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临床试验/NCT00693160
NCT00693160终止2 期

Effect of Intrathecal Ketorolac on Mechanical Hypersensitivity Following Acute Opioid Exposure

Wake Forest University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2007年12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
终止
入组人数
30
试验地点
1
主要终点
Hyperalgesia

研究概览

简要总结

This research study is being done because pain is a significant problem for patients with a variety of medical problems and following surgery or traumatic injury. Currently available pain medications may not treat all types of pain or may treat pain only at doses that produce side effects and complications. The medication in this study may have a role in better treatment of pain. The goals of this study are to see if a dose of ketorolac (non-narcotic, pain reliever), given into the fluid in the back near the spine has any effect on pain or discomfort in the skin sensation that will take place after applying capsaicin (chili pepper) cream. The sunburn-like sensation that people experience after having capsaicin cream applied is similar to, but much milder than, the pain that some people have after surgery and after certain types of nerve injuries. This study will test the effects of combining two medications that are often given together to control postoperative pain or pain from a nerve injury. The investigators are especially interested in answering two questions about the effects of ketorolac (non-narcotic pain reliever) and remifentanil (intravenous [IV] narcotic painkiller):

  1. How much does remifentanil (narcotic painkiller) affect the sunburn-like painful area on your skin, which develops after applying capsaicin cream?
  2. What pain relieving effects does spinal ketorolac have when given with IV remifentanil?

详细描述

Intravenous (IV) remifentanil stimulates spinal COX activity, leading to increased Cerebrospinal fluid CSF) prostaglandin E2 (PGE2) concentrations and areas of capsaicin-induced mechanical hypersensitivity after remifentanil infusion, and these effects will be blocked by intrathecal ketorolac.

Areas of mechanical hyperalgesia and allodynia will be established by topical capsaicin + intermittent heat in healthy volunteers, who will be randomized to receive intrathecal saline or ketorolac during remifentanil infusion, with primary outcome measure area of hyperalgesia and secondary outcome measure Cerebrospinal fluid (CSF) prostaglandin E2 (PGE2) concentration after stopping remifentanil.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiologist (ASA) I or II classification
  • between the ages of 18-55
  • weigh less than 250 pounds
  • without chronic pain

排除标准

  • taking analgesics in the last 2 weeks
  • positive urine drug screen
  • pregnancy
  • currently taking any prescription antidepressants or other medications that are mood altering
  • liver or kidney disease
  • stomach ulcers
  • allergies to ketorolac, lidocaine, or capsaicin cream
  • lung disease (COPD)

研究组 & 干预措施

Intrathecal Ketorolac

Experimental

In the presence of a remifentanil infusion subject will receive a single intrathecal injection of ketorolac 2 mg Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: ketorolac (Drug)

Intrathecal Ketorolac

Experimental

In the presence of a remifentanil infusion subject will receive a single intrathecal injection of ketorolac 2 mg Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: remifentanil (Drug)

Intrathecal Ketorolac

Experimental

In the presence of a remifentanil infusion subject will receive a single intrathecal injection of ketorolac 2 mg Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: Capsaicin (Drug)

Placebo intrathecal injection

Placebo Comparator

In the presence of remifentanil the subject will receive a single intrathecal injection of placebo (preservative-free normal saline) Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: placebo (Drug)

Placebo intrathecal injection

Placebo Comparator

In the presence of remifentanil the subject will receive a single intrathecal injection of placebo (preservative-free normal saline) Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: remifentanil (Drug)

Placebo intrathecal injection

Placebo Comparator

In the presence of remifentanil the subject will receive a single intrathecal injection of placebo (preservative-free normal saline) Each subject will receive the topical capsaicin model for hyperalgesia and allodynia assessment.

干预措施: Capsaicin (Drug)

结局指标

主要结局

Hyperalgesia

时间窗: 24 hours

Total Area of hypersensitivity (measured in centimeters) were assessed approximately 24 hours post intrathecal ketorolac injection by the method of using a von Frey filament

次要结局

  • Cerebrospinal Fluid (CSF) Prostaglandin E2 (PGE2) Concentration(2.5 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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