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Completed Phase 3 Interventional Results available

Efficacy of Dexlansoprazole MR on Heartburn Control in Participants Previously Receiving Twice Daily Proton Pump Inhibitor Therapy

ClinicalTrials.gov ID: NCT00847808

Public ClinicalTrials.gov record NCT00847808. 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 Jul 22, 2026, 4:10 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

A Phase 3b Multicenter, Single-Blind Trial to Evaluate the Efficacy of Dexlansoprazole MR 30 mg in Maintaining Control of Gastroesophageal Reflux Disease Symptoms in Subjects on Prior Twice Daily Proton Pump Inhibitor Therapy

Study identification

NCT ID
NCT00847808
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
178 participants

Conditions and interventions

Interventions

  • Dexlansoprazole MR QD Drug

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
Jan 31, 2009
Primary completion
Mar 31, 2010
Completion
Mar 31, 2010
Last update posted
Feb 2, 2012

2009 – 2010

United States locations

U.S. sites
52
U.S. states
26
U.S. cities
52
Facility City State ZIP Site status
Not listed Hueytown Alabama
Not listed Chandler Arizona
Not listed Sierra Vista Arizona
Not listed Tucson Arizona
Not listed Sherman Arkansas
Not listed Sherwood Arkansas
Not listed Carmichael California
Not listed Garden Grove California
Not listed Laguna Hills California
Not listed Long Beach California
Not listed Paramount California
Not listed Rancho Cucamonga California
Not listed Roseville California
Not listed Sacramento California
Not listed San Diego California
Not listed San Ramon California
Not listed Tustin California
Not listed Westlake Village California
Not listed Bristol Connecticut
Not listed Boynton Beach Florida
Not listed Hialeah Florida
Not listed New Smyrna Beach Florida
Not listed Winter Haven Florida
Not listed Augusta Georgia
Not listed Conyers Georgia
Not listed Newnan Georgia
Not listed Stockbridge Georgia
Not listed Rockford Illinois
Not listed Metairie Louisiana
Not listed Prince Frederick Maryland
Not listed Stevensville Michigan
Not listed Olive Branch Mississippi
Not listed Egg Harbor New Jersey
Not listed Albuquerque New Mexico
Not listed Rochester New York
Not listed Wilmington North Carolina
Not listed Columbus Ohio
Not listed Oklahoma City Oklahoma
Not listed Yukon Oklahoma
Not listed Portland Oregon
Not listed Lansdale Pennsylvania
Not listed Salisbury South Carolina
Not listed Chattanooga Tennessee
Not listed Johnson City Tennessee
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed El Paso Texas
Not listed Houston Texas
Not listed South Ogden Utah
Not listed Chesapeake Virginia
Not listed Norfolk Virginia
Not listed Lakewood Washington

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 NCT00847808, 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 Feb 2, 2012 · Synced Jul 22, 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 protocol, eligibility criteria, and contact information for NCT00847808 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →