Measuring pain intensity in healthy volunteers using different devices
Correlation of Pain Intensity Measurements in Healthy Volunteers Exposed to Unpleasant Stimuli
This study is testing two different devices to see how well they measure pain in healthy volunteers when they experience uncomfortable sensations.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 40 Years |
| Sex | All |
| Sponsor | Medical University of Gdansk Academic / other |
| Locations | 1 site (Gdansk, Pomeranian Voivodeship) |
| Trial ID | NCT06663761 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the correlation of pain intensity measurements in healthy volunteers exposed to unpleasant stimuli. It will compare two devices, PainMonitor and ANI Monitor, which assess pain through physiological parameters such as skin conductance. By analyzing how these devices respond to various stimuli, the study seeks to identify reliable and valid methods for measuring pain intensity. The findings could help improve pain assessment tools and enhance treatment strategies for pain management.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy volunteers aged 18 to 40 with an ASA general condition assessment of 1 or 2.
Not a fit: Patients with chronic pain conditions, arrhythmias, or those taking certain medications may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more accurate and reliable methods for assessing pain, ultimately improving patient care.
How similar studies have performed: While there have been various approaches to measuring pain, this specific comparison of physiological devices is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * American Society of Anesthesiology (ASA) general condition assessment 1 or 2 * age 18 - 40 yrs Exclusion Criteria: * any arrhythmia, * taking medications from the groups of beta-blockers, gabapentinoids, benzodiazepines, painkillers within the last 12 hours, * chronic pain conditions, * pregnancy, * trypanophobia (fear of needles)
Where this trial is running
Gdansk, Pomeranian Voivodeship
- Medical University of Gdansk - Departament of Anesthesiology and Intensive Care — Gdansk, Pomeranian Voivodeship, Poland (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.