Intravenous (IV) Pantoprazole in Erosive Esophagitis

• Sponsor: Emory University (Other)
• Overall Status: Completed
• CT.gov ID: NCT00133770
• Collaborator: Wyeth is now a wholly owned subsidiary of Pfizer (Industry)
• Enrollment: 20
• Location: 1
• Arm: 1
• Duration (Months): 32
• Patients Per Site Per Month: 0.6

Study Details

Study Description

Brief Summary

The aim of this study is to examine whether pantoprazole (Protonix) given through continuous intravenous infusion for 72 hours is superior to Protonix given through once a day IV injection in the treatment of erosive esophagitis.

Condition or Disease	Intervention/Treatment	Phase
Esophagitis	Drug: pantoprazole	Phase 4

Detailed Description

Gastroesophageal reflux disease (GERD) is a very common disease that affects 20-50% of adults in Western Countries. The disease can be divided into three clinical categories: nonerosive reflux disease (NERD), erosive reflux disease (ERD), and Barrett's esophagus.

Intravenous (IV) infusion produces a faster and steadier acid suppression than an oral regimen. Furthermore, some patients with severe erosive esophagitis cannot take pills by mouth and will benefit from an IV formulation. Recently, we observed healing of severe erosive esophagitis with continuous IV pantoprazole in several patients in 3 days. The safety of IV pantoprazole has been demonstrated in patients with GERD, with Zollinger-Ellison syndrome, or bleeding ulcer. This study is to define the safety and efficacy of continuous IV pantoprazole in the treatment of severe erosive esophagitis.

Comparison: The continuous IV pantoprazole compared to the once a day IV pantoprazole for 72 hours in the treatment of severe erosive esophagitis.

Study Design

• Study Type: Interventional
• Actual Enrollment: 20 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Pilot Study of Efficacy and Safety of Continuous Intravenous Infusion of Pantoprazole in the Treatment of Severe Erosive Esophagitis
• Study Start Date: Jul 1, 2004
• Actual Primary Completion Date: Jul 1, 2006
• Actual Study Completion Date: Mar 1, 2007

Arms and Interventions

Arm	Intervention/Treatment
Experimental: IV pantoprazole The continuous IV pantoprazole compared to the once a day IV pantoprazole for 72 hours in the treatment of severe erosive esophagitis	Drug: pantoprazole; The continuous IV pantoprazole compared to the once a day IV pantoprazole for 72 hours in the treatment of severe erosive esophagitis; Other Names: Protonix

Outcome Measures

Primary Outcome Measures

1. the percentage of patients healed from severe esophagitis with IV pantoprazole at 7 days [7 days]

   the percentage of patients healed from severe esophagitis with IV pantoprazole at 7 days

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Patients must be men or non-pregnant women (a documented negative pregnancy test at enrollment for females of child bearing age) at least 18 years of age

• Patients who present with a severe erosive esophagitis - confirmed by endoscopy (a baseline endoscopy within 24 hours of study enrollment) to be grade five or six, with or without stricture and/or ulcer

• Patients or their legally authorized representatives must be capable of understanding or giving signed and dated informed consent before the study

• Patients with a high probability for compliance and completion of the study

Exclusion Criteria:

• Patients with less than grade five esophagitis

• Patients with esophagitis other than reflux esophagitis, such as infectious esophagitis and esophageal cancer

• Patients who present with gastrointestinal bleeding, hematocrit decrease greater than 6 units or require more than 2 units transfusion at the presentation or during the time of the study

• Patients with severe comorbidities, such as liver diseases with asparate transaminase (AST) or alanine transaminase (ALT) greater than 3 times upper limit normal (ULN); alkaline phosphatase greater than 5 times the ULN; total bilirubin greater than 3.0 mg/dl; kidney diseases with serum creatinine greater than 2.0 mg/dl in men or 1.6 mg/dl in women; heart diseases; lung diseases; sepsis; and airway intubation.

• Patients with history of glaucoma in either eye; history of any intraocular eye surgery within preceding 3 months; history of, or presence of, signs of optic nerve swelling; history of acute change in vision; or vision loss in either eye.

• Patients with any malignancy (except skin cancer) which required therapy within the last 6 months

• Patients with history of allergy to any proton-pump inhibitor (PPI) including pantoprazole

• Patients with known human immunodeficiency virus infection

• Patients with organ transplantation

• Patients without the ability to comply with the study protocol and complete the study in the judgment of the investigator

• Patients with prior administration of any PPI (within 72 hours) or histamine-2 receptor antagonist (within previous 24 hours) of study enrollment

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Emory University School of Medicine	Atlanta	Georgia	United States	30322

Sponsors and Collaborators

• Emory University
• Wyeth is now a wholly owned subsidiary of Pfizer

Investigators

• Principal Investigator: Qiang Cai, MD, PhD, Emory University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Dr. Qiang Cai MD/PhD, Professor, Emory University
• ClinicalTrials.gov Identifier: NCT00133770
• Other Study ID Numbers: 259-2004; 3001K-200042
• First Posted: Aug 24, 2005
• Last Update Posted: Jul 31, 2013
• Last Verified: Jul 1, 2013

• Keywords provided by Dr. Qiang Cai MD/PhD, Professor, Emory University: IV pantoprazole; Esophagitis
• Additional relevant MeSH terms: Esophagitis; Pantoprazole

Study Results

No Results Posted as of Jul 31, 2013