跳至主要内容
临床试验/NCT01230463
NCT01230463Unknown不适用

Intraoperative Ketorolac Dose of 15 mg Versus the Standard 30 mg on Early Postoperative Pain After Spine Surgery: A Randomised, Blinded, Non-Inferiority Trial

University of Calgary1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2010年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
50
试验地点
1
主要终点
Visual Analog Score

研究概览

简要总结

The primary aim of this study is to show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery.

详细描述

Opioids have traditionally been the cornerstone of acute postoperative pain management. Problematic side effects such as nausea, vomiting, ileus, urinary retention, excess sedation, and respiratory depression are significant disadvantages with the use of opioids. Alternative treatments have been sought. The concept of adding a nonsedating non opioid analgesic agent is appealing and has been validated by previous studies. Nonsteroidal anti-inflammatory drugs (NSAID) are nonsedating and combine analgesic and anti-inflammatory properties ideal for pain after surgery.

Ketorolac is a potent intravenous nonsteroidal anti-inflammatory drug (NSAID), and a non selective cyclooxygenase inhibitor which mediates pain, inflammation and fever. It has been evaluated and used for treatment of moderate to severe pain including postoperative pain. Although intravenous route is not approved by Health Canada, its use is supported in medical literature and clinical practice.

Previous studies have demonstrated the effectiveness of standard 30 mg intravenous ketorolac as an adjunct to opioids for postoperative pain relief. Standard parenteral dose recommended by manufacturer for healthy non elderly population is 30 mg based on a number clinical trials.

Alberta Health Services (AHS) Pharmacy formulary has approved the intravenous use of ketorolac in the dosage range of 10-30 mg depending the patient's weight and medical comorbidities.

NSAIDs, including ketorolac, have an analgesic ceiling effect in which higher doses do not provide any additional pain relief but may increase the likelihood of side effects. Single dose IM ketorolac have been studied in the past showing no difference in analgesia with the 30 and 90 mg dose. Because of risk of drug toxicity and unwanted side effects, patients should be given the lowest effective ketorolac dose. Low dose ketorolac was studied in the adolescents undergoing spine surgery and showed that dose of 0.2mg/kg (11mg) provides supplemental analgesia postoperatively. However, there were no previous studies found on review of the literature using medline search that look at parallel comparison between intraoperative doses of ketorolac in terms of efficacy and safety profile.

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

  • Patients booked for 1-2 level spine laminectomies and/or decompression
  • Adult 18 - 65 years
  • Weight of 50 - 110 kg

排除标准

  • Previous lumbar laminectomy
  • Current anticoagulant use with INR > 1.2
  • Narcotic use > 4 weeks
  • Known allergy or sensitivity to NSAID or morphine
  • Renal insufficiency with creatinine >100 umol/L
  • Known liver disease
  • History of gastrointestinal bleeding
  • Pregnancy, history of bronchial asthma
  • NSAID use 2 days before surgery.

研究组 & 干预措施

15 mg ketorolac IV

Active Comparator

干预措施: Ketorolac Tromethamine (Drug)

30 mg ketorolac IV

Active Comparator

干预措施: Ketorolac Tromethamine (Drug)

结局指标

主要结局

Visual Analog Score

时间窗: Four hours after surgery

To show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery. Minimum clinically significant decrease in VAS pain score is 18 mm.

次要结局

  • Morphine Usage After Surgery(8 hours and 24 hours after surgery)
  • Morphine Adverse Effects(First 24 hours)
  • Postoperative Bleeding(24 hours after surgery)

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验