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Completed Phase 3 Interventional

Esomeprazole for Prevention of Upper Gastrointestinal Symptoms Associated With Continuous Use of NSAIDs

ClinicalTrials.gov ID: NCT00241514

Public ClinicalTrials.gov record NCT00241514. 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, 12:56 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

Efficacy of Esomeprazole 40 mg Once Daily Versus Placebo or Esomeprazole 20 mg Once Daily Versus Placebo in Prevention of Upper Gastrointestinal Symptoms Associated With Continuous Use of NSAIDs Including COX-2 Selective NSAIDs

Brief summary

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

This study was a multicentre, double-blind, randomised, placebo-controlled parallel group study consisting of 4 visits over a period of 6 months. The primary variable was to assess the efficacy of esomeprazole 40 mg orally qd (E40) or esomeprazole 20 mg orally qd (E20) versus placebo orally qd after 6 months of treatment for the prevention of relapse of upper GI symptoms associated with NSAID use, including COX-2 selective NSAIDs, in patients receiving daily NSAID therapy.

Study identification

NCT ID
NCT00241514
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
334 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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 2001 (Type not available)
Primary completion
Feb 2003 (Actual)
Completion
Feb 2003 (Actual)
Last update posted
Jan 21, 2011

2001 – 2003

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Research Site Tucson Arizona — —
Research Site Anaheim California — —
Research Site Orange California — —
Research Site San Francisco California — —
Research Site Bradenton Florida — —
Research Site Clearwater Florida — —
Research Site Fort Lauderdale Florida — —
Research Site Jacksonville Florida — —
Research Site South Miami Florida — —
Research Site West Palm Beach Florida — —
Research Site Zephyrhills Florida — —
Research Site Conyers Georgia — —
Research Site Newburgh Indiana — —
Research Site Baltimore Maryland — —
Research Site Winston-Salem North Carolina — —
Research Site Tulsa Oklahoma — —
Research Site Tipton Pennsylvania — —
Research Site Norfolk Virginia — —
Research Site Virginia Beach Virginia — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 94 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00241514, 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 21, 2011 · Synced Oct 23, 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 NCT00241514 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →