Migraine
Conditions
Brief summary
The purpose of this study is to test the effectiveness of an approved drug in the early treatment of migraine.
Interventions
Sponsors
Organon and Co
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Six month history of migraine; attacks typically mild when they begin with 1-4 migraine attacks per month.
Exclusion criteria
* Heart disease * High blood pressure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of patients who are pain free at 2 hours postdose | — |
| Tolerability as measured by subjective adverse experience reporting | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of patients with associated symptoms at 2 hours | — |
| Percentage of patients with 24 hour sustained pain freedom | — |
| Percentage of patients with functional disability at 2 hours | — |
| Percentage of patients requiring rescue medication between 2 & 24 hours | — |
| Percentage of patients pain free at 30/45/60/90 minutes post dose | — |
Outcome results
None listed