healthy volunteers
Conditions
Interventions
Oral administration of Ivabradine (5-15 mg) for 2 days
Oral administration of Placebo for 2 days
Sponsors
Shinshu University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: healthy adults volunteers
Exclusion criteria
Exclusion criteria: chronic pain history of heart failure electrocardiogram abnormality pregnant female regular use of analgesics neurologic deficits psychotic and depressive disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effects of Ivabradine on spontaneous pain produced by Capsaicin | — |
Secondary
| Measure | Time frame |
|---|---|
| Effects of oral administration of Ivabradine on the thermal hyperalgesia, mechanical hyperalgesia, mechanical allodynia, and flare produced by topical application of Capsaicin | — |
Countries
Japan
Contacts
Public ContactSatoshi Tanaka
Shinshu University School of Medicine Department of Anesthesiology and Resuscitology
Outcome results
None listed