ClinicalTrials.Veeva

Menu

H. Pylori Testing for Patients With Non-specific Upper Abdominal Pain in the Emergency Department

George Washington University (GW) logo

George Washington University (GW)

Status

Completed

Conditions

Gastritis
Peptic Ulcer
Stomach Ulcer
Peptic Ulcer Perforation

Treatments

Other: Urea Breath Test (UBT) for H. pylori infection

Study type

Observational

Funder types

Other

Identifiers

NCT01376414
IRB#: 111050

Details and patient eligibility

About

This pilot study aims to estimate the prevalence of Helicobacter pylori (H. pylori) colonization in patients presenting with non-specific abdominal pain (NSAP) in an urban academic emergency department (ED) located in Washington, DC.

Full description

The major goal is to study the prevalence of H. pylori using the 13C Urea Breath Test (UBT) in emergency department (ED) patients with non-specific abdominal pain. The investigators plan to enroll 250 patients during the pilot stage of this study. This T2 translational trial aims to apply recommended guidelines for the investigation and management of NSAP and dyspepsia into the practical arena of ED clinical care. The "test-and-treat" approach to symptomatic H. pylori infection has been endorsed by the American Gastroenterological Association (AGA). Patients who test positive for H. pylori by UBT will be treated with clarithromycin-based triple medication therapy as recommended by the American College of Gastroenterology (ACG) at the discretion of the treating physician. The rationale is that successful identification of H. pylori in the ED and initiation of treatment may reduce future risk of gastritis, gastric lymphoma, and gastric cancer, and is cost-effective through reduction of future healthcare costs and symptom severity. Study subjects will be followed for medication compliance, resolution of symptoms, and ability to obtain outpatient follow-up. As part of this study, the investigators will be collecting important information on the ED evaluation of abdominal pain.

Enrollment

212 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For any patient with chief complaint of "ABD", "STOM", "EPIG", "CHEST", "NAUS" "Do you have pain or discomfort or burning in your upper abdomen as the main reason for coming to ER today?"

Exclusion criteria

  • The patient LESS than 18 years old.
  • Patient does NOT speak English NOR has reliable adult translator.
  • Patient does NOT have capacity to give consent? (confused/intoxicated/etc.)
  • The patient currently is on antibiotics.
  • The patient currently is on a PPI. (eg. Prilosec [omeprazole]), protonix [pantoprazole], prevacid [lansoprazole], aciphex [rabeprazole], nexium [esomeprazole]
  • The patient has taken bismuth or pepto-bismol today.
  • The patient is known to be or suspected to be pregnant.
  • The patient UNABLE to walk to H.pylori Breath test.
  • The patient had "recent" negative H.pylori test for same symptoms.
  • There an "obvious alternative cause" for pain (per attending).

Trial design

212 participants in 1 patient group

Non specific upper abdominal pain
Description:
Cohort is patients who present to the Emergency Department with primary complaint of upper abdominal pain without obvious cause.
Treatment:
Other: Urea Breath Test (UBT) for H. pylori infection

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems