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Completed Phase 4 Interventional Results available

A Study to Determine the Effect of Sumatriptan and Naproxen Sodium Combination Tablet, Sumatriptan Tablet, and Naproxen Sodium Tablet on Blood Pressure When Treating Migraine Headaches That Occur During a 6-month Period

ClinicalTrials.gov ID: NCT00792636

Public ClinicalTrials.gov record NCT00792636. 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 26, 2026, 5:46 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

Assessment of the Effect of Sumatriptan and Naproxen Sodium Combination Tablet, Sumatriptan Tablet, and Naproxen Sodium Tablet Treatment on Blood Pressure When Administered Intermittently for Six Months for the Acute Treatment of Migraine Attacks, With or Without Aura, in Adults

Brief summary

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

The purpose of this study is to test the effect on blood pressure of sumatriptan and naproxen sodium combination tablets, tablets containing only sumatriptan, and tablets containing only naproxen sodium when these drugs are taken to treat migraine headaches that occur during a 6-month period.

Study identification

NCT ID
NCT00792636
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
407 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
Nov 2008 (Type not available)
Primary completion
Nov 2009 (Actual)
Completion
Nov 2009 (Actual)
Last update posted
Nov 23, 2016

2008 – 2009

United States locations

U.S. sites
49
U.S. states
19
U.S. cities
46
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 Phoenix Arizona 85050 —
GSK Investigational Site Tempe Arizona 85283 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Anaheim California 92801 —
GSK Investigational Site Anaheim California 92805 —
GSK Investigational Site Buena Park California 90620 —
GSK Investigational Site Garden Grove California 92845 —
GSK Investigational Site Newport Beach California 92660 —
GSK Investigational Site Santa Monica California 90404 —
GSK Investigational Site Westlake Village California 91361 —
GSK Investigational Site Colorado Springs Colorado 80904 —
GSK Investigational Site Avon Connecticut 06001 —
GSK Investigational Site Hialeah Florida 33010 —
GSK Investigational Site Jacksonville Florida 32216 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site Pembroke Pines Florida 33024 —
GSK Investigational Site St. Petersburg Florida 33702 —
GSK Investigational Site Sunrise Florida 33351 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Decatur Georgia 30034 —
GSK Investigational Site Chicago Illinois 60614 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Kalamazoo Michigan 49009 —
GSK Investigational Site Springfield Missouri 65807 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Greensboro North Carolina 27405 —
GSK Investigational Site Harrisburg North Carolina 28075 —
GSK Investigational Site Matthews North Carolina 28105 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Raleigh North Carolina 27612 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Cleveland Ohio 44122 —
GSK Investigational Site West Chester Ohio 45069 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Pittsburgh Pennsylvania 15236 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Simpsonville South Carolina 29681 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Memphis Tennessee 38018 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site San Antonio Texas 78205 —
GSK Investigational Site Salt Lake City Utah 84107 —
GSK Investigational Site West Jordan Utah 84088 —

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 NCT00792636, 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 Nov 23, 2016 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00792636 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →