healthy volunteers
Conditions
Interventions
Oral administration of Ivabradine
Oral administration of placebo
Sponsors
Shinshu University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: healthy humans
Exclusion criteria
Exclusion criteria: chronic pain analgesics within one month Electrocardiogram abnormality History of heart failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the increase in the mechanical, thermal, and electrical pain thresholds after oral administration of Ivabradine. | — |
Countries
Japan
Contacts
Public ContactSatoshi Tanaka
Shinshu University School of Medicine Department Anesthesiology and Resuscitology
Outcome results
None listed