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Completed Phase 3 Interventional

Efficacy/Safety of Lansoprazole in Patients With Frequent Heartburn

ClinicalTrials.gov ID: NCT00389948

Public ClinicalTrials.gov record NCT00389948. 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 21, 2026, 4:40 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

A Phase III, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial of 14 Day Treatment With Lansoprazole 15 mg Once a Day in Frequent Heartburn

Study identification

NCT ID
NCT00389948
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
576 participants

Conditions and interventions

Conditions

Interventions

  • Lanzoprazole 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
May 31, 2006
Primary completion
Not listed
Completion
Dec 31, 2006
Last update posted
Apr 15, 2007

2006 – 2007

United States locations

U.S. sites
28
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Clinical Research Consultants Inc. Hoover Alabama 35216
Not listed Huntsville Alabama 35802
Radiant Research Sierra Vista Arizona 85635
California Bio Medical Research Institute Los Angeles California 90025
Allergy Medical Group of North Area Roseville California 95678
Eastern Research Hialeah Florida 33013
Health Awareness Inc. Jupiter Florida 33458
Miami Research Associates Miami Florida 33173
Radiant Research Atlanta Georgia 30252
Radiant Research Atlanta Georgia 30308
Not listed Evansville Indiana 47714
Clinical Associates Reisterstown Maryland 21136
Medex Healthcare Research, Inc. St Louis Missouri 63117
Meridian Clinical Research LLC Omaha Nebraska 68134
William W. Anderson M.D. P.C. Rio Rancho New Mexico 87124
IRSI Port Chester New York 10573
Crescent Medical Research Salisbury North Carolina 28144
Micheal Alexander, DO Columbus Ohio 43204
New Hope Research of Oregon Portland Oregon 97219
Preferred Primary Care Physicians Carnegie Pennsylvania 15106
Advanced Therapeutics, Inc Johnson City Tennessee 37601
Nashville Medical Research Nashville Tennessee 37205
Medical Edge Healthcare Group, P.A. Dallas Texas 75243
Benchmark Research Fort Worth Texas 76135
Benchmark Research San Angelo Texas 76904
Commonwealth Clinical Research Specialist Richmond Virginia 23226
National Clinical Research Inc. Richmond Virginia 23294
Radiant Research Lakewood Washington 98499

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 NCT00389948, 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 Apr 15, 2007 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00389948 live on ClinicalTrials.gov.

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