Nexium 40mg Once Daily vs Prevacid 30mg Twice a Day for Control of Severe GERD

NCT ID: NCT00295685

Last Updated: 2009-02-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-10-31
• Study Completion Date: 2007-12-31

Brief Summary

The purpose of this study is to determine if people taking lansoprazole two times a day to control severe GERD symptoms can be controlled just as well, if not better, by taking Nexium just once a day.

Detailed Description

approximately 20% of patients taking first generation proton pump inhibitors (PPIs) are taking more than the standard approved dose. This dosing is required to attain adequate control of the gastric and intraesophageal pH in order to affect the desired clinical improvement. It is recognized that the b.i.d dosing strategy increases the intragastric pH control of <4 from approximately 12 hours to almost 16 hours. The refinement of the S isomer of omeprazole (Nexium)has led to a way to more effectively control acid exposure. Comparative trials with all the PPIs have shown significantly greater pH control of <4 and head to head comparisons as well as a recent crossover study. One study suggests that Nexium dosing contains approximately 16.5 hours of a pH control of <4. Conceivably, this duration of pH control suggests that b.i.d. dosing of other PPIs might be avoided. Furthermore, it suggests that patients currently taking b.i.d. PPIs might be successful candidates for conversion to q.d. Nexium. This would provide a considerable cost implication to health care plans and for patients who are responsible for paying for their PPI therapy. To date, esomeprazole has not been studied in comparison to b.i.d. dosing with other PPIs. There is pharmacologic evidence to suggest, however, that it is comparable. In this proposed study, we believe that by beginning with patients who were well controlled should make for a cleaner definition and a higher likelihood to demonstrate efficacy.

Conditions

GERD

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

Antacids

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Previous diagnosis of severe GERD.
• Male or female 18-80 years of age
• Ability to read, understand and provide informed consent
• GERD is Adequately controlled on BID lansoprazole as evidenced by GERD-HRQL score of </= 11
• Females of childbearing potential must use an acceptable method of birth control for the duration of the study.

Exclusion Criteria

• Known contraindications to Nexium
• Current or historical evidence of >3 cm histologically confirmed Barrett's metaplasia without current dysplasia, esophageal stricture or extraesophageal GERD symptoms.
• Previous Esophageal gastric surgery
• Pregnant or nursing Females
• Clinically significant abnormal laboratory values
• Medical condition that may be adversely impacted by participation in this study
• History of or current drug or alcohol abuse
• Known malignancy
• Need for concurrent therapy with any acid suppressive therapy other than the study drug, antacids, alginates, NSAIDS, >165 mg ASA, prostaglandin analogs, prokinetic drug, antineoplastic agents, Ketoconazole, Itraconazole, Voriconazole, Clarithromycin, Telithromycin, HIV protease inhibitors, Rifampin, Phenobarbital, or Digoxin
• Use of investigational drug or experimental device within 30 days prior to screening

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

Digestive & Liver Disease Specialists

OTHER

Sponsor Role: lead

Principal Investigators

David A Johnson, MD

Role: PRINCIPAL_INVESTIGATOR

Digestive & Liver Disease Specialists

Locations

Digestive & Liver Disease Specialists

Norfolk, Virginia, United States

Countries

United States

Other Identifiers

IRUSESOM0159

Identifier Type: -

Identifier Source: org_study_id