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Characterization of bimodal electrocutaneous stimulation

Characterization of bimodal electrocutaneous stimulation - Bimodal electrocutaneous stimulation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30433
Enrollment
25
Registered
2007-05-01
Start date
2007-05-23
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Chronische Pijn Chronic pain

Interventions

None listed

Sponsors

Universtiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Right-handedness Age 18 - 30 yrs

Exclusion criteria

Exclusion criteria: Pain complaints for more than 1 week during previous 3 months Pain complaints during the experiments Psychotropic medication Skin disease on upper extremity

Design outcomes

Primary

MeasureTime frame
Sensation threshold for both stimulus modes, subjective reports concerning intensity (weak/strong) and quality (dull/sharp), EP peak amplitudes and the difference of these parameters per person measured at two insances of time.

Secondary

MeasureTime frame
Not appicable

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)