192
Participants
Start Date
September 30, 2005
Primary Completion Date
February 28, 2006
Study Completion Date
February 28, 2006
Frovatriptan
"This study employed a prospective, non-randomized, open-label single-sequence design. The study was conducted in two phases:~1. A Usual Care phase (approximately 1 month in duration) included one menstrual period during which female patients treated all episodes of migraine headaches using their current treatment (referred to as the Baseline phase in the protocol)~2. An Acute Treatment phase (approximately 1 month in duration), following the Usual Care phase, included one menstrual period during which female patients used frovatriptan 2.5 mg to treat all episodes of migraine headache when their headache reached IHS Grade 1. If needed, a second dose of frovatriptan 2.5 mg was administered; however, this second dose could not be administered within 2 hours of the initial dose (i.e., there must have been at least 2 hours between doses of frovatriptan). The total daily dose of frovatriptan was not to exceed 3 tablets over a 24-hour period."
Usual Care
Current treatment used to treat all migraine headaches
Stratford
Clearwater
Jacksonville
Largo
Tampa
Blackwood
New York
Plainview
Vestal
Burlington
Raleigh
Salisbury
Winston-Salem
Cincinnati
West Chester
Norristown
Philadelphia
Saint Petersburg
Upland
Nashville
Houston
Lead Sponsor
Endo Pharmaceuticals
INDUSTRY