het onderzoek betreft gezonde vrijwilligers waarbij wordt gekeken op de mate van opgewekte experimentele pijn na toediening van een medicament. experimental pain
Conditions
Interventions
Volunteers will be randomly assigned to either first placebo group and a couple
of weeks later treatment group or vice versa. All volunteers will undergo in
total two series of pain tests: one treat
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: healthy volunteers of both sexes in the age range of 18-75 years.
Exclusion criteria
Exclusion criteria: Unable to give written informed consent Medical disease such as renal, liver, cardiac, vascular (incl. hypertension) or infectious disease History of cerebro-vascular accident 30)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| amount of pain expressed as e-VAS (electronic Visual Analoge Scale). | — |
Countries
Netherlands
Outcome results
None listed