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Prediction of Acute Postoperative Pain and Analgesic Consumption (MIRPEX-3)

K

Kasper Grosen

Status

Unknown

Conditions

Postoperative Pain

Study type

Observational

Funder types

Other

Identifiers

NCT02230865
MIRPEX-3

Details and patient eligibility

About

Pain is an expected part of surgical recovery but effective pain management remains challenging. The high variability in postoperative pain experience and analgesic treatment response between patients is part of the challenge. Few studies have yet combined preoperative assessment of responses to experimental pain with measurements of cognitive and emotional processes in the prediction of postoperative pain.

We hypothesize, that preoperative evoked brain potentials (using standard electroencephalographic brain imaging), endogenous pain inhibition capacity (conditioned pain modulation), responses to pressure/thermal pain stimulation, and/or situational pain-related catastrophic thinking are useful clinical predictors of postoperative pain and analgesic consumption.

Full description

Preselected preoperative predictor variables/individual patient characteristics include the following:

  • Evoked brain potentials (using standard electroencephalographic brain imaging)
  • Capacity of descending pain inhibition induced by a cold pressor test (2C in 120 sec)
  • Pressure pain detection and tolerance thresholds in muscle (m.quadriceps)
  • Pressure pain tolerance thresholds in bone (sternum and tibia)
  • Heat pain tolerance threshold in skin (forearm)
  • Responses to the Situational and Dispositional Pain Catastrophizing Scale
  • Response to the State-Trait and Anxiety Inventory
  • Response to the Beck's Depression Inventory

Enrollment

40 estimated patients

Sex

Male

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective minimally invasive surgical correction of funnel chest (pectus excavatum
  • age ≥15 years.

Exclusion criteria

  • Previous thoracic surgical interventions
  • Presence of diseases affecting the central and/or peripheral nervous system
  • Presence of chronic pain conditions
  • Inability to speak and/or understand Danish
  • Inability to understand and participate in the experimental pain session
  • Presence of psychiatric disorders
  • History of frostbite in the non-dominant upper limb
  • Presence of sores or cuts on non-dominant upper limb
  • Presence of cardiovascular disease
  • History of fainting and/or seizures
  • Presence of fractures of the non-dominant upper limb
  • Presence of Reynaud's phenomenon.

Secondary exclusions included:

  • Insensitivity to experimental cold pressor pain
  • Lack of epidural catheter placement
  • Re-operation

Trial design

40 participants in 1 patient group

Surgery
Description:
Minimally invasive repair of pectus excavatum

Trial contacts and locations

1

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Central trial contact

Kasper Grosen, MHSc, PhD; Asbjørn M Drewes, MD, PhD, DMSci

Data sourced from clinicaltrials.gov

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