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Immediate Detection of Helicobacter Infection With a New Electrochemical System.

Primary Purpose

H. Pylori Infection

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Electrochemical H. pylori detection method
IHC
C13-urea breath test
HUT
Sponsored by
University of Erlangen-Nürnberg Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for H. Pylori Infection

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Written informed consent
  • Age 18-85 years
  • Ability of subjects to understand character and individual consequences of clinical trial
  • Subjects undergoing EGD

Exclusion Criteria:

  • Inability to provide written informed consent
  • Severe Coagulopathy (Prothrombin time < 50% of control, Partial thromboplastin time > 50 s)
  • Pregnancy or breast feeding
  • Active gastrointestinal bleeding
  • Residing in institutions (e.g. prison)
  • PPI intake
  • antibiotic use, actual or within the last 4 weeks

Sites / Locations

  • University of Erlangen-Nuremberg

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

H. pylori positive patients

H. pylori negative patients

Arm Description

Outcomes

Primary Outcome Measures

Effectiveness of the newly developed device in comparison to IHC, HUT and C13-urea breath test.

Secondary Outcome Measures

Full Information

First Posted
November 2, 2010
Last Updated
December 10, 2020
Sponsor
University of Erlangen-Nürnberg Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT01234389
Brief Title
Immediate Detection of Helicobacter Infection With a New Electrochemical System.
Official Title
Immediate Detection of Helicobacter Infection With a New Electrochemical System
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
October 2009 (Actual)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Erlangen-Nürnberg Medical School

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Helicobacter pylori-infection (H. pylori) affects about fifty percent of the general population and is associated with peptic ulcer disease, non-cardia gastric adenocarcinoma and gastric lymphoma. Currently, diagnostic methods include breath tests, serology, stool antigen tests, histology or the Helicobacter urease test (HUT). The aim of our study is to access the clinical reliability of a new, electrochemical device for rapid H. pylori detection.
Detailed Description
The newly developed electrochemical device for H. pylori detection consists of a working and reference electrode between which a biopsy sample is administered. Afterwards, acquired voltage-values could be analysed for characteristics typical for H. pylori infection (ammonia). According to Sydney classification, biopsies are taken from gastric antrum and corpus for electrochemical H. pylori detection, HUT and immunohistochemistry (IHC). HUT results are evaluated after 24 hours. Furthermore, every patient will receive 13C-urea breath test. IHC is designated as the gold standard of H. pylori diagnosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
H. Pylori Infection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
H. pylori positive patients
Arm Type
Other
Arm Title
H. pylori negative patients
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
Electrochemical H. pylori detection method
Intervention Description
Determination of H. pylori infection.
Intervention Type
Device
Intervention Name(s)
IHC
Other Intervention Name(s)
Determination of H. pylori infection.
Intervention Description
Determination of H. pylori infection.
Intervention Type
Device
Intervention Name(s)
C13-urea breath test
Intervention Description
Determination of H. pylori infection.
Intervention Type
Device
Intervention Name(s)
HUT
Intervention Description
Determination of H. pylori infection.
Primary Outcome Measure Information:
Title
Effectiveness of the newly developed device in comparison to IHC, HUT and C13-urea breath test.
Time Frame
Oktober 2009 - February 2011

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Written informed consent Age 18-85 years Ability of subjects to understand character and individual consequences of clinical trial Subjects undergoing EGD Exclusion Criteria: Inability to provide written informed consent Severe Coagulopathy (Prothrombin time < 50% of control, Partial thromboplastin time > 50 s) Pregnancy or breast feeding Active gastrointestinal bleeding Residing in institutions (e.g. prison) PPI intake antibiotic use, actual or within the last 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markus F. Neurath, M.D., Ph.D.
Organizational Affiliation
University of Erlangen-Nürnberg
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Helmut Neumann, M.D., Ph.D.
Organizational Affiliation
University of Erlangen-Nürnberg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Erlangen-Nuremberg
City
Erlangen
State/Province
Bayern
ZIP/Postal Code
91054
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

Immediate Detection of Helicobacter Infection With a New Electrochemical System.

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