跳至主要内容
临床试验/NCT00354029
NCT00354029已完成4 期

Effect of Perioperative i.v. Low-dose S(+) Ketamine in Patients Undergoing Hemorrhoidectomy

Asker & Baerum Hospital1 个研究点 分布在 1 个国家目标入组 83 人开始时间: 2006年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
83
试验地点
1
主要终点
NRS Pain = Numeric Rating Scale (0-10)

研究概览

简要总结

The purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine reduces the amount and degree of postoperative pain.

Furthermore the purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine effects cognitive function in the early postoperative period.

详细描述

The mechanism of development of postoperative pain is complex. Central and peripheral sensitization are playing an important role and this can lead to postoperative hypersensitization. Several studies have shown, that S (+) ketamine can be effective to reduce sensitization and postoperative pain. Ketamine (2-O-chlorophenyl-2-methylamino cyclohexanone) is a N-Methyl-D-Aspartat (NMDA) receptor antagonist. S (+) ketamine has a four times stronger affinity to the NMDA receptor compared to R (-) ketamine. The duration of action for S (+) ketamine is shorter than R (-) ketamine and it has fewer side-effects.

The purpose of this study is to compare the analgetic effect of pregabalin and placebo used in the perioperative period.

The hypothesis is that perioperative intravenous S (+) ketamine gives significant better analgesia than placebo without effecting cognitive function.

The study is including patients undergoing hemorrhoidectomy.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of disc prolapse
  • ASA (American Society in Anesthesiology) I-II
  • written consent

排除标准

  • Age < 18
  • ASA > II
  • liver failure
  • renal failure
  • heart failure
  • pregnancy

研究组 & 干预措施

Placebo

Placebo Comparator

Saline 0,9%

干预措施: Placebo (Drug)

S (+) Ketamine

Active Comparator

干预措施: S (+) Ketamine (Drug)

结局指标

主要结局

NRS Pain = Numeric Rating Scale (0-10)

时间窗: 24 hours

The numeric rating scale (NRS) is used to measure the intensity of pain. The value 0 means no pain and the value 10 represents maximal pain. a higher intensity of pain is associated with a worse outcome.

次要结局

未报告次要终点

研究者

发起方
Asker & Baerum Hospital
申办方类型
Other

研究点 (1)

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