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临床试验/NL-OMON49357
NL-OMON49357已完成不适用

Transitional Pain Service for patients at Risk of chronic postsurgical pain Undergoing Surgery - The TRUSt study

Academisch Medisch Centrum0 个研究点目标入组 180 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
已完成
入组人数
180

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. Patients aged 18 years or older
  • 2. Willing and able to provide informed consent
  • 3. Undergoing a surgical procedure with an increased risk of CPSP (amputation,
  • spinal surgery, thoracotomy, breast surgery, herniotomy, hysterectomy and after
  • arthroplasty) (8).
  • Any surgical procedure and one of the following:
  • - Diagnosed chronic pain, defined according to the ICD-11 as *an unpleasant
  • sensory and emotional experience associated with actual or potential tissue
  • damage, or described in terms of such damage. Chronic pain is pain that
  • persists or recurs for longer than 3 months (3)*
  • - Chronic opioid use, defined as > 20 mg daily morphine equivalent (MME)
  • consumption for more than 3 months in the last 3 months
  • - Allergy to opioid agents
  • - Patients with pain device implants, such as intrathecal pain pump, spinal
  • cord stimulation or peripheral nerve stimulator
  • - The usage of pain medication as methadone, buprenorphine, anticonvulsants,
  • antidepressants or medicinal cannabis for chronic pain for more than 3 months
  • in the last three months
  • - Psychosocial comorbidities like anxiety, depression, pain catastrophizing if
  • documented in the electronic medical record

排除标准

  • - Not willing or able to provide written informed consent
  • - Emergency surgery

研究者

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