跳至主要内容
临床试验/EUCTR2014-005701-20-NL
EUCTR2014-005701-20-NL进行中(未招募)不适用

Shifting pain modulation towards anti-nociceptivity: Mechanism-specific pharmacological prevention of post sternotomy pain: the MASTER study - MASTER

eiden University Medical Center0 个研究点开始时间: 2015年2月2日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients of either sex with American Society of Anesthesiologists score 1, 2 or 3, aged 18 to 70 years planned to undergo elective surgery involving a sternotomy may be enrolled in the study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 290
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • 1. Pain scores > 3 (on a 11-point numerical rating scale, NRS) reported for most of the day during the past month (including angina);
  • 2. The presence of any chronic pain disorder;
  • 3. Regular use of analgesics for any purpose, including SNRIs, gabapentinoids, COX inhibitors or NSAIDs during the previous month;
  • 4. Use of MAO-inhibitors within the last 14 days;
  • 5. The presence of narrow-angle glaucoma;
  • 6. Inability to perform psychophysical testing (eg. in case of cognitive or psychiatric disorders);
  • 7. Patients suffering from cognitive dysfunction;
  • 8. Patients being treated for depression, or any other mood disorder;
  • 9. Inability to give informed consent;
  • 10. Inability to communicate with the investigators;
  • 11. Known allergies to the study medication:
  • 12. Uncontrolled hypertension (diastolic blood pressure > 100 mmHg).

研究者

发起方
eiden University Medical Center

相似试验