pain patient and healthy volunteers
Conditions
Interventions
None listed
Sponsors
Division of Dental Anesthesiology, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: after informed consent is obtained, over 16 years old
Exclusion criteria
Exclusion criteria: the inability to give informed consent, under 16 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the modulation of CPM in pain patient compared to the helthy volunteers (CPM effect: Evaluation of CPM effect is assessed by Quantitative Sensory Testing (QST) such as Pressure Pain threshold measured by pressure algometer or threshold measured by von Frey filament as subjective evaluation. The CPM effect is evaluated during and after conditioning stimulation. CPM effect is defined as ratio of pain threshold of TS during CS to pain threshold before application of CS (baseline).) | — |
Secondary
| Measure | Time frame |
|---|---|
| the modulation of QST (the Thermal Pain Illusion(TPI), Temporal Summation(TS), Offset Analgesia(OA) etc) and the effect of background (for example, psychology test including SDS, STAI, PCS etc), analgesics and the stress evaluated by Catecholamine concentrations in plasma, urine and sweat in pain patient compared to the healthy volunteers | — |
Countries
Japan
Contacts
Public ContactYuka Oono
Department of Diagnostic and Therapeutic Sciences, School of Dentistry, Meikai University Division of Dental Anesthesiology
Outcome results
None listed