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Completed Phase 4 Interventional

An Open-Label Study of Once-Daily Oral Administration of Esomeprazole 40 mg in Patients With Symptoms of Gastroesophageal Reflux Disease (GERD)

ClinicalTrials.gov ID: NCT00242736

Public ClinicalTrials.gov record NCT00242736. 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, 2:31 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 of Once-Daily Oral Administration of Esomeprazole 40 mg in Patients With Symptoms of Gastroesophageal Reflux Disease (GERD) to Investigate the Relationship Between the Presence of Erosive Esophagitis (EE) at Baseline and Heartburn Resolution After 4 Weeks of Treatment

Brief summary

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

The purpose of this study is to evaluate whether there is a difference in proportion of patients with resolution of heartburn and other symptoms related to gastroesophageal reflux disease (GERD) after four weeks of treatment with esomeprazole (NEXIUM®) in those subjects with Erosive Esophagitis (EE) and those without EE.

Study identification

NCT ID
NCT00242736
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
350 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Oct 2005 (Type not available)
Primary completion
Not listed
Completion
Jan 2006 (Actual)
Last update posted
Mar 6, 2009

2005 – 2006

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
25
Facility City State ZIP Site status
Research Site Alabaster Alabama — —
Research Site Mobile Alabama — —
Research Site Tucson Arizona — —
Research Site North Little Rock Arkansas — —
Research Site Anaheim California — —
Research Site Orange California — —
Research Site Torrance California — —
Research Site Miami Florida — —
Research Site Ocoee Florida — —
Research Site Tampa Florida — —
Research Site Zephyrhills Florida — —
Research Site Arlington Heights Illinois — —
Research Site New Orleans Louisiana — —
Research Site Shreveport Louisiana — —
Research Site Hollywood Maryland — —
Research Site Elkin North Carolina — —
Research Site Oklahoma City Oklahoma — —
Research Site Chattanooga Tennessee — —
Research Site Knoxville Tennessee — —
Research Site Austin Texas — —
Research Site Houston Texas — —
Research Site Ogden Utah — —
Research Site Salt Lake City Utah — —
Research Site Christiansburg Virginia — —
Research Site Norfolk Virginia — —

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 NCT00242736, 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 Mar 6, 2009 · Synced Oct 26, 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 NCT00242736 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →