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Clinical Trials/NL-OMON26410
NL-OMON26410Not yet recruitingNot Applicable

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

Amsterdam University Medical Center, location Meibergdreef (AMC)0 sites180 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
180
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

/A

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •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

Exclusion Criteria

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

Investigators

Sponsor
Amsterdam University Medical Center, location Meibergdreef (AMC)

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