RecruitingACTRN12607000474459

Observational trial of correlations between skin conductance and postoperative pain in children


Sponsor

Associate Professor Thomas Ledwoski

Enrollment

180 participants

Start Date

Aug 7, 2007

Study Type

Observational

Conditions

Summary

Up to today, there is no gold standard available for the assessment of pain in young children after operations. Aim of this trial is to investigate the correlation between pain obtained by behavioural or nurse rated assessment with skin conductance readings obtained at the same time. We hope that by that means we may be able to measure pain objectively and be able to conclude about wether or not a child requires acute pain relief. We will include 180 patients in 3 age groups (1-3, 4-7 and 8-16 yrs) and observe their pain (nurse assessed, behavioural, self assessed) in the recovery room. At the same time we will obtain skin conductance readings via 3 sticky dots on the hand (a method which itself is absolutely pain-free). From these readings we will try to find correlations or certain patterns that might allow conclusion about the level of pain by simple skin conductance assessment.


Eligibility

Sex: Both males and femalesMin Age: 1 YearsMax Age: 16 Yearss

Plain Language Summary

Simplified for easier understanding

This study is looking at whether a simple, painless test that measures sweating on the hand (called skin conductance) can help us understand how much pain a child is feeling after surgery. Right now, accurately measuring pain in young children — especially toddlers who cannot explain how they feel — is very difficult. Researchers will measure skin conductance using small sticky sensors on the hand at the same time that nurses assess pain using standard tools. The goal is to see if skin conductance could one day be used as an objective, pain-free way to measure a child's pain level. You may be eligible if: - Your child is between 1 and 16 years old - Your child is recovering from surgery in the post-anaesthesia recovery room You may NOT be eligible if: - Your child has developmental delay - Your child has a syndrome or major systemic medical condition - Your child takes medicines that affect the autonomic nervous system (such as anticholinergics, antidepressants, or ADHD medications) - Your child is classified as ASA category 3 or 4 (high anaesthetic risk) - Your child's hands are not accessible - Your child has a known reaction to adhesive patches Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Once the patients arrive in the recovery room, skin conductance will be assessed via 3 standard electrocardiogram (ECG) electrodes on the hand. The correlation of these measures with the pain score of

Once the patients arrive in the recovery room, skin conductance will be assessed via 3 standard electrocardiogram (ECG) electrodes on the hand. The correlation of these measures with the pain score of the patients at the same time will be assessed. The assessment is limited to the time the patients spend in the recovery room.


Locations(1)

Australia

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ACTRN12607000474459