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Treatment of Zollinger-Ellison Syndrome With Prevacid

C

Charles Mel Wilcox, MD

Status and phase

Completed
Phase 4

Conditions

Zollinger-Ellison Syndrome
Multiple Endocrine Neoplasia

Treatments

Drug: Lansoprazole (Prevacid)

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00204373
F030107005

Details and patient eligibility

About

The purpose of this study is to study the safety and efficacy of high dose Prevacid in the long-term treatment of patients who secrete abnormally large amounts of gastric acid.

Full description

The aim of this protocol is to study the medical management of acid hypersecretory states including Zollinger-Ellison using Prevacid. The immediate objective is to heal peptic ulcers and eliminate symptoms and in the long term to prevent relapse of symptoms, lesions and complications. Other objectives include observation of the efficacy in controlling gastric acid production and of the safety of high dose, long-term use of Prevacid.

Enrollment

72 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with Zollinger-Ellison syndrome

Exclusion criteria

  • Pregnant or lactating females

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

72 participants in 1 patient group

single group
Experimental group
Description:
This is an open label, non-randomized, uncontrolled, single group study designed to treat patients with Zollinger-Ellison Syndrome and other hypersecretory conditions by controlling gastric acid production; to heal and prevent relapses of peptic ulcers and symptoms; to monitor the safety and efficacy of this treatment.
Treatment:
Drug: Lansoprazole (Prevacid)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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