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Completed Phase 3 Interventional Results available

TREXIMET® Versus Butalbital-containing Combination Medications for the Acute Treatment of Migraine in Adults

ClinicalTrials.gov ID: NCT00573170

Public ClinicalTrials.gov record NCT00573170. 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, 2:33 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

A Randomized, Double-blind, Double-dummy, Placebo-controlled, Crossover Study to Evaluate the Efficacy of TREXIMET® (Sumatriptan + Naproxen Sodium) vs. Butalbital-containing Combination Medications for the Acute Treatment of Migraine When Administered During the Moderate-Severe Migraine Pain, Studies 1 and 2 of 2

Brief summary

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

Study TRX109011/TRX109013, A Randomized, Double-blind, Double-dummy, Placebo-controlled, Crossover Study to Evaluate the Efficacy of TREXIMET® (Sumatriptan + Naproxen Sodium) versus Butalbital-containing Combination Medications (BCM) for the Acute Treatment of Migraine when administered during the Moderate-Severe Pain Phase of the Migraine (Studies 1 and 2 of 2)

Study identification

NCT ID
NCT00573170
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
375 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
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
Feb 2008 (Type not available)
Primary completion
Aug 2009 (Actual)
Completion
Aug 2009 (Actual)
Last update posted
Dec 29, 2010

2008 – 2009

United States locations

U.S. sites
107
U.S. states
33
U.S. cities
97
Facility City State ZIP Site status
GSK Investigational Site Chandler Arizona 85224 —
GSK Investigational Site Gilbert Arizona 85234 —
GSK Investigational Site Litchfield Park Arizona 85340 —
GSK Investigational Site Mesa Arizona 85213 —
GSK Investigational Site Phoenix Arizona 85014 —
GSK Investigational Site Tempe Arizona 85283 —
GSK Investigational Site Little Rock Arkansas 72201 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Anaheim California 92801 —
GSk Investigational Site Anaheim California 92805 —
GSK Investigational Site Garden Grove California 92845 —
GSK Investigational Site Irvine California 92618 —
GSK Investigational Site Newport Beach California 92660 —
GSK Investigational Site Northridge California 91325 —
GSK Investigational Site Riverside California 92501 —
GSK Investigational Site Sacramento California 92585 —
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site San Francisco California 94109 —
GSK Investigational Site Santa Monica California 90404 —
GSK Investigational Site Sherman Oaks California 91403 —
GSK Investigational Site Walnut Creek California 94596 —
GSK Investigational Site Westlake Village California 91361 —
GSK Investigational Site Colorado Springs Colorado 80909 —
GSK Investigational Site East Hartford Connecticut 06118 —
GSK Investigational Site New Britain Connecticut 06050 —
GSK Investigational Site Clearwater Florida 33755 —
GSK Investigational Site Daytona Beach Florida 32117 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Naples Florida 34102 —
GSK Investigational Site Pembroke Pines Florida 33024 —
GSK Investigational Site Plantation Florida 33324 —
GSK Investigational Site West Palm Beach Florida 33407-2450 —
GSK Investigational Site Atlanta Georgia 30309 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Rome Georgia 30165 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Suwanee Georgia 30024 —
GSK Investigational Site Chicago Illinois 60614 —
GSK Investigational Site Gurnee Illinois 60031 —
GSK Investigational Site Maywood Illinois 60153 —
GSK Investigational Site Indianapolis Indiana 46256 —
GSK Investigational Site Paducah Kentucky 42003 —
GSK Investigational Site Shreveport Louisiana 71101 —
GSK Investigational Site Shreveport Louisiana 71103 —
GSK Investigational Site Biddeford Maine 04005 —
GSK Investigational Site Pikesville Maryland 21208 —
GSk Investigational Site Brockton Massachusetts 02301 —
GSK Investigational Site Springfield Massachusetts 01104 —
GSK Investigational Site Ann Arbor Michigan 48104 —
GSK Investigational Site Kalamazoo Michigan 49009 —
GSK Investigational Site Hattiesburg Mississippi 39401 —
GSK Investigational Site Springfield Missouri 65807 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Henderson Nevada 89014 —
GSK Investigational Site Las Vegas Nevada 89119 —
GSK Investigational Site Cherry Hill New Jersey 08002 —
GSK Investigational Site Ridgewood New Jersey 07550 —
GSK Investigational Site Stratford New Jersey 08084 —
GSK Investigational Site Albuquerque New Mexico 87108 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site Brooklyn New York 11235 —
GSK Investigational Site Mount Vernon New York 10550 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10022 —
GSK Investigational Site Orchard Park New York 14127 —
GSK Investigational Site Schenectady New York 12308 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Valley Stream New York 11580 —
GSK Investigational Site Cary North Carolina 27518 —
GSK Investigational Site Charlotte North Carolina 28204 —
GSK Investigational Site Greenville North Carolina 27858 —
GSK Investigational Site Hickory North Carolina 28601 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Bismarck North Dakota 58501 —
GSK Investigational Site Fargo North Dakota 58104 —
GSK Investigational Site Minot North Dakota 58704 —
GSK Investigational Site Cincinnati Ohio 45227 —
GSK Investigational Site Cincinnati Ohio 45245 —
GSK Investigational Site Cleveland Ohio 44122 —
GSK Investigational Site Columbus Ohio 43210 —
GSK Investigational Site Dayton Ohio 45406 —
GSK Investigational Site Toledo Ohio 43614-5809 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Greensburg Pennsylvania 15601 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Philadelphia Pennsylvania 19114 —
GSK Investigational Site Pittsburgh Pennsylvania 15236 —
GSK Investigational Site Warwick Rhode Island 02886 —
GSK Investigational Site Beaufort South Carolina 29902 —
GSK Investigational Site Charleston South Carolina 29412 —
GSK Investigational Site Simpsonville South Carolina 29681 —
GSk Investigational Site Rapid City South Dakota 57702 —
GSK Investigational Site Columbia Tennessee 38401 —
GSK Investigational Site Cordova Tennessee 38018 —
GSK Investigational Site Germantown Tennessee 38139 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Austin Texas 78745 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75234 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site San Antonio Texas 78258 —
GSK Investigational Site Salt Lake City Utah 84107 —
GSK Investigational Site Virginia Beach Virginia 23452 —

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 NCT00573170, 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 Dec 29, 2010 · Synced Oct 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00573170 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →