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临床试验/NL-OMON48981
NL-OMON48981招募中不适用

EFFECTS OF TAPENTADOL ON CHRONIC PAIN AND PARAMETERS OF CENTRAL SENSITIZATION. A PROSPECTIVE, OPEN LABEL, RANDOMIZED CROSS-OVER STUDY WITH PREGABALIN AS COMPARATOR, - PRINCE

niversitair Medisch Centrum Groningen0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Gender: female
  • 2. Age: 18 years and older
  • 3. Presence of proven endometriosis or CLBPr
  • 4. Signs of central sensitization
  • 5. No contraindications for opioids or pregabalin.
  • 6. Signed informed consent.

排除标准

  • 1. No or insufficient understanding of Dutch language.
  • 2. Incapacity to follow instructions.
  • 3. Mental incompetence to provide informed consent.
  • 4. CLBP with radiation to both legs.
  • 5. Pain in one (or more) sites where QST will be applied.
  • 6. Usage of opioids with more powerful spectre, such as oxycodone, fentanyl, morphine in the week prior to start of the study.
  • 7. Previous usage of pregabalin or tapentadol
  • 8. Alcohol abuse.
  • 9. Pregnancy or woman who wish to be pregnant.
  • 10. Kidney and/or liver function disturbances in patients with a medical history (<6 months) of kidney and liverdisturbances

研究者

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