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临床试验/NL-OMON26410
NL-OMON26410尚未招募不适用

Transitional Pain Service for patients at Risk of chronic postsurgical pain Undergoing Surgery

Amsterdam University Medical Center, location Meibergdreef (AMC)0 个研究点目标入组 180 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
180

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • 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) (9).
  • 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

发起方
Amsterdam University Medical Center, location Meibergdreef (AMC)

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