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Clinical Trials/NL-OMON54413
NL-OMON54413
Completed
Not Applicable

PJ-008200 Measurements on healthy subjects to design a nociception index - Measurements to design a nociception index

Philips Patient Monitoring (Philips Medizin-Systeme Böblingen GmbH)0 sites40 target enrollmentTBD
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Conditionsmeten van pijn bij gezonde vrijwilligersNociceptionPain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
meten van pijn bij gezonde vrijwilligers
Sponsor
Philips Patient Monitoring (Philips Medizin-Systeme Böblingen GmbH)
Enrollment
40
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
Philips Patient Monitoring (Philips Medizin-Systeme Böblingen GmbH)

Eligibility Criteria

Inclusion Criteria

  • •1\) Age between 18 and 65 years old
  • •2\) ASA I Healthy subjects
  • •3\) BMI \< 35
  • •4\) Females should be using contraception

Exclusion Criteria

  • •1\) Pregnancy (pregnancy test before start protocol, if female, with the
  • •exception of post menstrual women)
  • •2\) Smoking
  • •3\) Alcohol abuse
  • •4\) Medication that influeunces the central or peripheral nervous system, or the
  • •cardiovascular system
  • •5\) Drug use (drug test before start protocol)
  • •6\) Raynaud's disease (poor blood circulation)
  • •7\) Scleroderma, Dupuytren\*s Contracture, or other Rheumatology issues
  • •8\) Depression and/or anxiety (the Hospital Anxiety and Depression Scale (HADS)

Outcomes

Primary Outcomes

Not specified

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