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Monitoring of Skin Conductance to Assess Postoperative Pain Intensity

Non-randomized, observational trial to assess correlations between skin conductance and postoperative pain in the recovery room

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12606000166572
Enrollment
75
Registered
2006-05-10
Start date
2006-05-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Previous investigations have shown that a relatively new method of skin conductance assessment (SC) correlates with periods of stress and pain (one of which might be during the period of recovery after anaesthesia) during an operation. The method follows the “lie detector principle”: the electric skin conductance is assessed by three self-sticking electrodes placed on the palm of the hand. People who are stressed often experience “sweaty palms” (due to changes in the autonomous nervous system that results in an increased filling of sweat glands). The wetter the palms, the higher the skin conductance recorded. We would like to compare the method of SCA to the results of score based pain assessment, like a visual analogue scale, during the recovery period after general anaesthesia. In this study we will recruit 75 patients. The patients will receive a standard anaesthesia and postoperative care. The SCA uses three ECG electrodes placed on the palmar surface of the hand. It is safe and not painful. We will not interfere with the anaesthesia or postoperative pain control in any way, but will observe the monitored data to get an idea about how well it correlates with our normal score based pain assessment. For that purpose, a nurse who is blinded to the readings of the skin conductance monitor will ask the patient to rate his pain on a numeric rating scale (0-10), as normally done to rate a patient's pain level in the recovery room. A second observer will record the results from the monitor ast the same time. The study will hopefully help to develop a better monitoring device for the assessment of postoperative pain. This might help with patients who have difficulties in expression of pain, for example, due to language problems or confusion.

Interventions

No intervention; we will observe the changes in skin conductance (measured by 3 electrodes at the palmar surface of the hand) in the postoperative period (meanwhile the patient is in the recovery room, so for approximately about 20 to 120 minutes) and its correlation with postoperative pain. Each single measurement will take approximately 10 seconds.

Sponsors

Dr. Thomas Ledowski
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients > 18 yrs, male and female patients.

Exclusion criteria

Pacemaker, betavlocker, atropine/glycopyrrolate medication, inability to communicate in English.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026