Standard Triple Therapy vs Sequential Therapy in Treatment of H Pylori Infection



Status:Completed
Conditions:Infectious Disease
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 85
Updated:4/2/2016
Start Date:February 2012
End Date:January 2013
Contact:Byron Cryer, MD
Email:byron.cryer@utsouthwestern.edu
Phone:214-857-1603

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Conventional Therapy vs Sequential Therapy for the Treatment of Helicobacter Pylori Infection

Traditionally, H pylori infection has been treated with conventional triple therapy. This
includes amoxicillin, clarithromycin and a proton pump inhibitor all given daily for 10-14
days. In Europe, the guidelines now advocate treatment of H pylori with sequential therapy
which is 5 days of amoxicillin therapy with proton pump inhibitor followed by 5 days of
clarithromycin, metronidazole, and proton pump inhibitor with better response rates. We
hypothesize that H. pylori resistance pattern and treatment response rates observed in
Europe will not be predictive of resistance patterns and response rates in the United
States.


Inclusion Criteria:

Subject has signed informed consent Subject is an adult older than 18 yrs old and requires
an upper endoscopic evaluation If female and of child bearing potential, subject has a
negative pregnancy test and is not nursing.

Patient has not received prior treatment for H pylori Subject is able to understand and
comply with study procedures

Exclusion Criteria:

Recent use (within 4 weeks) of any of the medications used in the treatment of H
pylori(Amoxicillin, Clarithromycin, Metronidazole) Subject undergoing endoscopy for acute
gastrointestinal bleeding Subject has an allergy to any of the medications used in the
treatment of H pylori Subject has a history of esophageal or gastric carcinoma including
lymphoma Subject has esophageal varices or undergoing endoscopy for esophageal banding
Subject is taking warfarin or clopidogrel Subject has coagulopathy that precludes safe
biopsy of the biopsy areas Subject has comorbidity that precludes safe participation in
the study Subject is a pregnant female Subject has a history of H. pylori infection.
Patient is already enrolled in GI Study. History of UGI surgery other than Nissen
Fundoplication
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