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COMPLETED Phase 4

An Open Label pH Comparison of Esomeprazole and Lansoprazole in Barrett's Esophagus Patients

NCT00352261 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to compare the treatment of esomeprazole 40 mg once daily and lansoprazole 30 mg once daily in controlling intragastric pH in Barrett's Esophagus patients

Conditions Studied

Interventions

  • DRUG Esomeprazole
  • DRUG Lansoprazole

Study Locations (12)

Arizona

  • Research Site — Phoenix
  • Research Site — Tucson

Missouri

  • Research Site — Kansas City
  • Research SIte — Springfield

Illinois

  • Research Site — North Chicago

Minnesota

  • Research Site — Rochester

Montana

  • Research Site — Butte

Ohio

  • Research Site — Cleveland

Pennsylvania

  • Research Site — Philadelphia

Tennessee

  • Research Site — Knoxville

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2006-01
Est. Completion 2007-04
Phase Phase 4

Sponsor

AstraZeneca

1,053 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00352261

The ClinicalTrials.gov registry entry for NCT00352261 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,053 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Barrett's Esophagus appearing as the primary indexed condition, and to 2 interventions — of which Esomeprazole is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00352261 reports 12 study locations spanning 10 distinct geographic areas — top geographies include Arizona, Missouri, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00352261 about?

NCT00352261 is a clinical study titled "An Open Label pH Comparison of Esomeprazole and Lansoprazole in Barrett's Esophagus Patients". The purpose of the study is to compare the treatment of esomeprazole 40 mg once daily and lansoprazole 30 mg once daily in controlling intragastric pH in Barrett's Esophagus patients

What is the current status of trial NCT00352261?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2006-01. Estimated completion is 2007-04.

What conditions does trial NCT00352261 study?

This clinical trial studies the following conditions: Barrett's Esophagus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00352261?

The interventions under investigation include: Esomeprazole (DRUG), Lansoprazole (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00352261?

This trial is sponsored by AstraZeneca, which has 1,053 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00352261 being conducted?

This trial has 12 study locations across Arizona, Illinois, Minnesota, Missouri, Montana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial