Effectiveness And Safety Of Frovatriptan For The Management (Acute Treatment) Of Menstrual Migraine

PHASE4CompletedINTERVENTIONAL
Enrollment

192

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

February 28, 2006

Study Completion Date

February 28, 2006

Conditions
Menstrual Migraine (MM) Headaches
Interventions
DRUG

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."

DRUG

Usual Care

Current treatment used to treat all migraine headaches

Trial Locations (21)

Unknown

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

Sponsors
All Listed Sponsors
lead

Endo Pharmaceuticals

INDUSTRY