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Prediction of Acute Postoperative Pain and Analgesic Consumption

Prediction of Acute Postoperative Pain and Analgesic Consumption by Preoperative Responses to Experimental Pain in Patients Undergoing Chest Wall Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02230865
Acronym
MIRPEX-3
Enrollment
40
Registered
2014-09-03
Start date
2014-08-31
Completion date
2015-06-30
Last updated
2015-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

Funnel chest (Pectus excavatum)

Brief summary

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.

Detailed 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

Interventions

None listed

Sponsors

Kasper Grosen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
15 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain intensityWithin the first 5 days after surgery11-point (0-10) numerical rating scale of pain intensity
Postoperative pain unpleasantnessWithin the first 5 days after surgery11-point (0-10) numerical rating scale of pain unpleasantness
Postoperative consumption of analgesicsWithin the first 5 days after surgeryThe use of all pain-related treatments, including rescue analgesics and any other concomitant pain treatments.

Countries

Denmark

Contacts

Primary ContactKasper Grosen, MHSc, PhD
kasper.grosen@rm.dk78464224
Backup ContactAsbjørn M Drewes, MD, PhD, DMSci
amd@rn.dk97660000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026