NL-OMON49357已完成不适用
Transitional Pain Service for patients at Risk of chronic postsurgical pain Undergoing Surgery - The TRUSt study
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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