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Completed Phase 4 Interventional Accepts healthy volunteers Results available

"Completeness of Response" Following Treatment With Treximet™ for Migraine

ClinicalTrials.gov ID: NCT00893737

Public ClinicalTrials.gov record NCT00893737. 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 19, 2026, 9:08 AM EDT

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

Official title

An Open-label Study to Evaluate "Completeness of Response" Following Treatment With Treximet™ for Migraine

Brief summary

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

Many clinical trials may not fully explore criteria that are important to some migraine patients' definition of "complete response." This study offers the opportunity to evaluate the effectiveness of Treximet™ when non-standard criteria are examined (for example, neck pain, irritability or fatigue). Subjects enrolled at 8 investigative sites will complete 2 visits. Subjects will complete a Completeness of Response Survey at Visit 1 considering their usual migraine medication (a triptan) and a Completeness of Response Survey at Visit 2 considering their study medication (Treximet™).

Study identification

NCT ID
NCT00893737
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Cady, Roger, M.D.
Individual
Enrollment
147 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Jun 2009 (Type not available)
Primary completion
Jan 2010 (Actual)
Completion
Jan 2010 (Actual)
Last update posted
Jan 25, 2011

2009 – 2010

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
San Francisco Clinical Research Center San Francisco California 94109 —
Westside Family Medical Center Kalamazoo Michigan 49009 —
Clinvest Springfield Missouri 65807 —
Mercy Health Research/Ryan Headache Center St Louis Missouri 63141 —
Island Neurological Associates, PC Plainview New York 11803 —
Preferred Primary Care Physicians Pittsburgh Pennsylvania 15236 —
Wesley Headache Clinic and Research Center Cordova Tennessee 38018 —
Texas Headache Associates San Antonio Texas 78258 —

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 NCT00893737, 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 Jan 25, 2011 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00893737 live on ClinicalTrials.gov.

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