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Completed Phase 4 Interventional

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

ClinicalTrials.gov ID: NCT00904098

Public ClinicalTrials.gov record NCT00904098. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 11:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Females 18 years of age or older with at least one year history of menstrual migraine (MM) headaches participated in a Phase 4 clinical trial to evaluate the efficacy of frovatriptan when used at the early stage (International Headache Society \[IHS\] Grade 1) of MM compared with patients' current treatment.

Study identification

NCT ID
NCT00904098
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
192 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2005 (Type not available)
Primary completion
Feb 2006 (Actual)
Completion
Feb 2006 (Actual)
Last update posted
Feb 15, 2010

2005 – 2006

United States locations

U.S. sites
21
U.S. states
9
U.S. cities
21
Facility City State ZIP Site status
Not listed Stratford Connecticut — —
Not listed Clearwater Florida — —
Not listed Jacksonville Florida — —
Not listed Largo Florida — —
Not listed Tampa Florida — —
Not listed Blackwood New Jersey — —
Not listed New York New York — —
Not listed Plainview New York — —
Not listed Vestal New York — —
Not listed Burlington North Carolina — —
Not listed Raleigh North Carolina — —
Not listed Salisbury North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed West Chester Ohio — —
Not listed Norristown Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Saint Petersburg Pennsylvania — —
Not listed Upland Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Houston Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00904098, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 15, 2010 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00904098 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →