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Completed Phase 3 Interventional

Treximet (Sumatriptan/Naproxen Sodium), Formerly Known as TREXIMA, for Menstrual Migraine in Women With Dysmenorrhea

ClinicalTrials.gov ID: NCT00329459

Public ClinicalTrials.gov record NCT00329459. 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 23, 2026, 3:16 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, Single Migraine Attack, Placebo -Controlled, Patallel-group Multicenter Study to Evaluate the Efficacy and Tolerability or Trexima (Sumatriptan Succinate/Naproxen Sodium) Tablets vs Placebo When Administered During the Mild Pain Phase of Menstrual Migraine in Women With Dysmenorrhea

Brief summary

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

This study was designed to determine efficacy of TREXIMA compared to placebo for the treatment of a menstrual migraine.

Study identification

NCT ID
NCT00329459
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
320 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
May 2006 (Type not available)
Primary completion
Nov 2006 (Actual)
Completion
Nov 2006 (Actual)
Last update posted
Oct 24, 2016

2006

United States locations

U.S. sites
34
U.S. states
22
U.S. cities
34
Facility City State ZIP Site status
GSK Investigational Site Mesa Arizona 85201 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fair Oaks California 95628 —
GSK Investigational Site Newport Beach California 92660 —
GSK Investigational Site San Diego California 92128 —
GSK Investigational Site San Francisco California 94102 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Fort Lauderdale Florida 33328 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Milford Massachusetts 01757 —
GSK Investigational Site North Dartmouth Massachusetts 02747 —
GSK Investigational Site Detroit Michigan 48201 —
GSK Investigational Site Springfield Missouri 65804 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Moorestown New Jersey 08057 —
GSK Investigational Site Albuquerque New Mexico 87102 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site Plainview New York 11803 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site Greensboro North Carolina 27401 —
GSK Investigational Site Cleveland Ohio 44195 —
GSK Investigational Site Independence Ohio 44131 —
GSK Investigational Site Westerville Ohio 43081 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Pittsburgh Pennsylvania 15236 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Memphis Tennessee 38018 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Salt Lake City Utah 84121 —
GSK Investigational Site Wenatchee Washington 98801 —

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 NCT00329459, 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 Oct 24, 2016 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00329459 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →