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Prediction of Chronic Pain by the Pain Monitor

Prediction of the Occurrence of Chronic Pain After Thoracotomy by Measuring Preoperative Skin Conductance (Pain Monitor Device)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01595711
Acronym
D3C
Enrollment
6
Registered
2012-05-10
Start date
2012-03-07
Completion date
2013-09-07
Last updated
2018-01-29

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

Conditions

Surgery

Brief summary

The skin conductance algesimeter (Pain Monitor™, Med-Storm Innovation AS, NO-0264 Oslo, Norway)) reflects the sympathetic nervous system by the measurement of the skin conductance of the palm of the hand. SCA detects nociceptive pain fast and continuously, specific to the individual, with higher sensitivity and specificity than other available objective methods. The skin conductance response to a calibrated noxious stimulus varies among patients. It defines two types of people depending on its magnitude. The investigators assume that the importance of skin conductance response to a noxious stimulus predicts the occurrence of chronic pain in patients operated by thoracotomy.

Interventions

Measurement of cutaneous conductance

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* adult patients of both sexes * planned pulmonary resection for cancer performed by a posterolateral thoracotomy * thoracic epidural analgesia

Exclusion criteria

* pregnancy, * morbid obesity, * insulin-dependent diabetes with dysautonomia, * inability to proceed with anesthesia using the BIS signal, * known allergy to remifentanil, propofol, atracurium or to levobupivacaine, * contra-indication to nefopam * contra-indication to ketoprofen

Design outcomes

Primary

MeasureTime frameDescription
Prediction of chronic painone year after surgeryPrediction of chronic pain by the measurement of skin conductance

Secondary

MeasureTime frameDescription
Prediction of the postoperative pain5 days postoperativelyPrediction of the postoperative pain by the measurement of skin conductance. Postoperative pain is assessed (pain score) at least twice each day at rest and during mobilisation.
Prediction of the postoperative antalgic requirement5 days postoperativelyPrediction of the postoperative analgesic requirement by the measurement of skin conductance. The analgesic requirement is evaluated by the amount of epidural analgesics.
Prediction of the postoperative antalgic requirement by the genetic studyOne year after surgeryPrediction of the postoperative antalgic requirement by the genetic study
Effect of remifentanil on skin conductanceOne hour after anesthesiaSkin conductance is measured before and after a calibrated noxious stimulus. This test is performed after the induction of anesthesia (propofol) and a first time before remifentanil administration and a second time after.

Countries

France

Outcome results

None listed

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