Rapid Urease Test for Diagnosis of H. Pylori Infection in Patients With Peptic Ulcer Bleeding
Primary Purpose
Peptic Ulcer, Hemorrhage
Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
endoscopic biopsy
endoscopic biopsy
endoscopic biopsy
Sponsored by
About this trial
This is an interventional diagnostic trial for Peptic Ulcer focused on measuring peptic ulcer, hemorrhage, rapid urease test, urea breath test
Eligibility Criteria
Inclusion Criteria:
- gastroduodenal ulcer with bleeding, documented by endoscopic examination
Exclusion Criteria:
- 1. receiving continuous proton pump inhibitor treatment, antibiotics within 4 weeks 2. not suitable for endoscopic biopsy 3. hemodynamically unstable
Sites / Locations
- Far Eastern Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
A1
A4
B1
Arm Description
one biopsy specimen taken from gastric antrum was put into RUT kit
4 biopsy specimens taken from gastric antrum were put into RUT kit
one biopsy specimen taken from gastric body was put into RUT kit
Outcomes
Primary Outcome Measures
the sensitivity of rapid urease test for H. pylori
the sensitivity of rapid urease test for H. pylori using 13C-UBT as gold standard
Secondary Outcome Measures
Full Information
NCT ID
NCT01282853
First Posted
January 23, 2011
Last Updated
August 28, 2015
Sponsor
Far Eastern Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01282853
Brief Title
Rapid Urease Test for Diagnosis of H. Pylori Infection in Patients With Peptic Ulcer Bleeding
Official Title
The Influence of Biopsy Number and Site on the Sensitivity of Rapid Urease Test for Diagnosis of H. Pylori Infection in Patients With Bleeding Gastroduodenal Ulcer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2011
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Far Eastern Memorial Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Rapid urease test (RUT) is the most commonly used biopsy-based method to diagnose Helicobacter pylori (Hp) infection because of its simple, rapid and accurate characters. However, its sensitivity was reported to decrease during ulcer bleeding recently. So it is an important issue to avoid a false negative test in these patients. Siddique et al reported that the sensitivity of RUT could be increased when the biopsy number increased from 1 to 4. Other studies demonstrated that additional biopsy from gastric body would increased the sensitivity of RUT in patients with ulcer bleeding. Therefore, we design this study to see if increased number of biopsy or different location of biopsy could increase sensitivity of RUT in patients with gastroduodenal ulcer bleeding.
After receiving explanation and giving consent, these patients with gastric or duodenal ulcer bleeding diagnosed after endoscopic examination will be enrolled. Those who are unstable, have received antibiotic or continuous proton pump inhibitor treatment within 4 weeks, or are contraindicated for endoscopic biopsy will be excluded. We will take 1 piece, 4 pieces of biopsy samples from prepyloric antrum and 1 piece from gastric body with standard biopsy forceps from the patients after they agree for RUT test. Then, we put these samples into 3 separate RUT kits respectively. We use 13C-UBT as gold standard for diagnosis of Hp infection. It is scheduled: (1) if the condition of this patient is not suitable for breath test just after endoscopic examination, 13C-UBT will be performed within 2 days,(2) otherwise, it will be performed 1 hour after examination. We plan to enroll 100 patients for this study. We will apply McNamer's test to examine the difference of RUT sensitivity of different biopsy number. For the RUT sensitivity from different locations, we use kappa statistic method to analyze their consistency.
Detailed Description
as brief summary
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer, Hemorrhage
Keywords
peptic ulcer, hemorrhage, rapid urease test, urea breath test
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
116 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A1
Arm Type
Active Comparator
Arm Description
one biopsy specimen taken from gastric antrum was put into RUT kit
Arm Title
A4
Arm Type
Experimental
Arm Description
4 biopsy specimens taken from gastric antrum were put into RUT kit
Arm Title
B1
Arm Type
Experimental
Arm Description
one biopsy specimen taken from gastric body was put into RUT kit
Intervention Type
Procedure
Intervention Name(s)
endoscopic biopsy
Other Intervention Name(s)
HelicotecUT plus for rapid urease test
Intervention Description
endoscopic biopsy for rapid urease test
Intervention Type
Procedure
Intervention Name(s)
endoscopic biopsy
Other Intervention Name(s)
HelicotecUT plus for rapid urease test
Intervention Description
endoscopic biopsy for rapid urease test
Intervention Type
Procedure
Intervention Name(s)
endoscopic biopsy
Other Intervention Name(s)
HelicotecUT plus for rapid urease test
Intervention Description
endoscopic biopsy for rapid urease test
Primary Outcome Measure Information:
Title
the sensitivity of rapid urease test for H. pylori
Description
the sensitivity of rapid urease test for H. pylori using 13C-UBT as gold standard
Time Frame
within 2 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
gastroduodenal ulcer with bleeding, documented by endoscopic examination
Exclusion Criteria:
1. receiving continuous proton pump inhibitor treatment, antibiotics within 4 weeks 2. not suitable for endoscopic biopsy 3. hemodynamically unstable
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tzong-Hsi Lee, MD
Organizational Affiliation
Far Eastern Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Far Eastern Memorial Hospital
City
New Taipei city
ZIP/Postal Code
22060
Country
Taiwan
12. IPD Sharing Statement
Learn more about this trial
Rapid Urease Test for Diagnosis of H. Pylori Infection in Patients With Peptic Ulcer Bleeding
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