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Clinical Trials/DRKS00022324
DRKS00022324
Completed
N/A

Assessing alterations in sensation after peripheral nerve injuries

Klinik für Unfallchirurgie, UMG0 sites21 target enrollmentJune 29, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
G54.0
Sponsor
Klinik für Unfallchirurgie, UMG
Enrollment
21
Status
Completed
Last Updated
last year

Overview

Brief Summary

Vibrotactile sensation is an essential part of the sense of touch. In this study, the localized vibrotactile sensation of the arm-shoulder region was quantified in 10 able-bodied subjects. For this analysis, the six relevant dermatomes (C3-T2) and three segments—the lower arm, the upper arm, and the shoulder region were studied. For psychometric evaluation, tasks resulting in the quantification of sensation threshold, just noticeable difference, Weber fraction, and perception of dynamically changing vibrotactile stimuli were performed. We found that healthy subjects could reliably detect vibration in all tested regions at low amplitude (2–6% of the maximal amplitude of commonly used vibrotactors). The detection threshold was significantly lower in the lower arm than that in the shoulder, as well as ventral in comparison with the dorsal. There were no significant differences in Weber fraction (20%) detectable between the studied locations. A compensatory tracking task resulted in a significantly higher average rectified error in the shoulder than that in the upper arm, while delay and correlation coefficient showed no difference between the regions. Here, we presented a conclusive map of the vibrotactile sense of the healthy upper limb. These data give an overview of the sensory bandwidth that can be achieved with vibrotactile stimulation at the arm and may help in the design of vibrotactile feedback interfaces (displays) for the hand/arm/shoulder-region.

Registry
who.int
Start Date
June 29, 2020
End Date
July 23, 2021
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Klinik für Unfallchirurgie, UMG

Eligibility Criteria

Inclusion Criteria

  • Upper\-limb amputees, brachial plexus injured subject subjects suffering chronic regional pain syndrome and volunteering healthy subjects aged between 18 and 80 years will be included in the study. No gender preference is applied. The subject has to have legal capacity to give the consent at his/her own will.

Exclusion Criteria

  • Diabetes mellitus
  • Delicate skin conditions or skin lesions
  • Polyneuropathy
  • Pregnancy
  • Current immunosuppressive treatment
  • Addictive behavior defined as the abuse of cannabis, opioids or other drugs
  • Carrier of infectious diseases
  • Inability to cooperate

Outcomes

Primary Outcomes

Not specified

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