ClinicalTrials.gg
Status unknownNCT05046990MOTIVATIONUpdated Mar 1, 2023

Arrangement of Collecting Venules for the Endoscopic Diagnosis of Helicobacter Pylori

An observational study in Helicobacter Pylori Infection, sponsored by Hospital Clinic of Barcelona. Status unknown at 5 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-03-01.

Sponsored by Hospital Clinic of Barcelona · Observational

The sponsor has not verified this record recently (last verified Dec 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000
Ages
18 Years and older
Sex
All
01

Study summary

To perform a prospective, observational, international, multicentre, in vivo study to assess the performance of regular arrangement of collecting venules (RAC) for the exclusion of Helicobacter pylori (Hp) infection using white light high definition (HD) endoscopy without any kind of zoom or magnification.

Gold standard will be mucosal biopsies (Sydney protocol) or urease test. Immunohistochemistry (IHC) should be performed in case of a negative histologic study for Hp in patients taking proton pump inhibitors (PPIs).

Participants will perform a training test with 20 pictures of the distal part of the lesser curvature before starting the inclusion of cases.

Secondary objectives are:

  • To assess whether age, sex and PPIs, have an influence on the results of RAC.
  • To assess the correlation of atrophic gastritis and intestinal metaplasia (confirmed in histopathological samples) and RAC.
  • To assess reproducibility of RAC on real time examinations with different operators and in different countries with different Hp infection prevalence.

Primary and secondary variables

The primary study variable is:

- Endoscopic detection of RAC.

Secondary variables will be considered:

  • Sex
  • Age
  • PPI intake in the last two weeks
  • Centre
  • Country
  • Hp prevalence
  • Endoscopist
  • Type of endoscope
  • Significant findings (need of histological confirmation)

    • Atrophic gastritis
    • Intestinal metaplasia
    • Erosive gastritis
    • Benign gastric ulcer
    • Gastric adenoma
    • Gastric cancer
Read the detailed description

This is a prospective, multicentre, international study without a control group.

Training phase Before starting the inclusion of patients, 20 HD images previously collected by the principal investigator will be sent to each of the study investigators. Pictures will clearly show the RAC pattern present or absent at the level of the distal gastric lesser curvature. In case of doubtful RAC, the pattern shall be considered negative. Investigators will be able to discuss their questions and doubts after the training phase (videoconference).

Endoscopic examination Upper endoscopy will be performed with HD endoscopes and a high-definition screen. Two endoscopists will participate in each hospital. The examination will be performed according to the protocol of each centre. Visualisation of the entire oesophageal, gastric and duodenal surface will be performed as in routine clinical practice. The presence of RAC will be assessed during the gastric exploration with sufficient insufflation and its detection will be considered as the presence of a regular starfish-shaped erythematous punctation in the lower part of the lesser curvature of the gastric body, close to the incisura angularis.

In case of the presence of residues in the gastric cavity that prevent the correct visualisation of the area, water washings shall be performed for the correct characterisation of the mucosa. At least one photo of the described gastric region shall be taken with the image processor system to maintain its high-definition quality. All the data (name, date of birth, clinical record number, date of exploration…) will be removed from the picture to ensure the anonymisation. Subsequently, the photographs will be downloaded and saved in a folder on a network drive of each hospital.

After characterisation of the gastric mucosa, the Hp infection status will be assessed by taking biopsies with a standard forceps for anatomopathological study according to Sydney's protocol (2 in the antrum, 1 in the incisura and 2 in the body). Ideally, biopsies for a urease test will also be obtained.

Histopathological examination Samples shall be fixed in formalin and analysed by the Anatomical Pathology service for histological examination by haematoxylin and eosin (H\&E) and special staining for Hp (e.g. modified Giemsa). In patients taking PPI, if Hp is negative in the H\&E histological study, the study will be completed by immunohistochemical (IHC) staining.

02

Conditions studied

  • Helicobacter Pylori Infection
03

In context

Lead sponsor

Hospital Clinic of Barcelona is the lead sponsor of 326 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

Patients older than 18 years without previous history of Hp infection or eradication undergoing a gastroscopy in each center

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients older than 18 years without previous history of Hp infection or eradication undergoing a gastroscopy

Exclusion criteria

Exclusion Criteria:

  • Patients taking oral anticoagulants (acenocoumarol and new anticoagulants as dabigatran, rivaroxaban, apixaban and edoxaban), NSAIDs or with intake of antibiotics in the last 4 weeks, but aspirin at a dose of 100 mg per day will be included
  • Diseases that affect the gastric mucosa and preclude the evaluation of the collecting venules pattern (portal hypertension, gastric lymphoma)
  • History of previous gastric cancer or patients in surveillance for preneoplastic lesions (atrophic gastritis/IM),
  • Previous gastric surgery,
  • Active bleeding or presence of blood or food that would impede a complete mucosal evaluation.
  • Negative to participate in the study or inability to provide signed consent
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • RAC evaluation

    Patients older than 18 years without previous history of Hp infection or eradication undergoing a gastroscopy

    Diagnostic Test: Regular Arrangement of Collecting Venules

Interventions

  • Diagnostic testRegular Arrangement of Collecting Venules

    This is a prospective, multicentre, international study without a control group.

06

What researchers measure

Primary outcomes

  1. RAC performance

    A total of 1000 consecutive patients with no history of Hp who come for gastroscopy will be included in the study to perform a prospective, observational, international, multicentre, in vivo study to assess the performance of regular arrangement of collecting venules (RAC). Endoscopists will perform a training test with 20 pictures of the distal part of the lesser curvature before starting the inclusion of cases. 17 different centers will participate in the study and each of them will include between 50 and 100 patients. Presence of RAC using white light high definition endoscopy without magnification determines the exclusion of Helicobacter pylori (Hp) infection. Gold standard diagnosis test for Hp infection will be histological results by mucosal biopsies (Sydney protocol) or urease test. Immunohistochemistry (IHC) should be performed in case of a negative histologic study for Hp in patients taking proton pump inhibitors (PPIs).

    Time frame: 12 months

Secondary outcomes

  1. Baseline characteristics

    To assess whether age, sex and PPIs, have an influence on the results of RAC in all patients.

    Time frame: 12 months

  2. Histological correlation

    To assess the correlation of atrophic gastritis and intestinal metaplasia (confirmed in histopathological samples) and RAC in all patients.

    Time frame: 12 months

  3. Reproducibility

    To assess reproducibility of RAC on real time examinations with different operators and in different countries with different Hp infection prevalence.

    Time frame: 12 months

07

Study locations

3 of 5 sites recruiting
  • Cliniques Universitaires Saint Luc
    Brussels, 1080, Belgium
    Recruiting
  • München University Hospital
    Munich, Bavaria 80331, Germany
    • Riccardo Vasapolli, MD · Contact
    Recruiting
  • Hospital de Mérida
    Mérida, Badajoz 06800, Spain
    Completed
  • Hospital de Viladecans
    Viladecans, Barcelona 08840, Spain
    Active, not recruiting
  • Hospital Clinic de Barcelona
    Barcelona, 08036, Spain
    Recruiting
08

References and documents

Publications

  • Garces-Duran R, Galdin-Ferreyra M, Delgado-Guillena PG, Cuatrecasas M, Cordova H, Garcia-Rodriguez A, Rodrigo-Calvo MT, Jimeno-Ramiro M, Araujo IK, Gines A, Llach J, Fernandez-Esparrach G. Diagnosis of Helicobacter pylori Infection by the Arrangement of Collecting Venules Using White Light Endoscopy: Evaluation of Interobserver Agreement. Dig Dis. 2022;40(3):376-384. doi: 10.1159/000518100. Epub 2021 Jun 30. PubMed 34348294 ↗
  • Garces-Duran R, Garcia-Rodriguez A, Cordova H, Cuatrecasas M, Gines A, Gonzalez-Suarez B, Araujo I, Llach J, Fernandez-Esparrach G. Association between a regular arrangement of collecting venules and absence of Helicobacter pylori infection in a European population. Gastrointest Endosc. 2019 Sep;90(3):461-466. doi: 10.1016/j.gie.2019.05.027. Epub 2019 May 17. PubMed 31108089 ↗

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05046990
Responsible party
Sponsor
First posted
Sep 16, 2021
Start date
Dec 1, 2021
Primary completion
Jun 30, 2023 (estimated)
Completion
Sep 30, 2023 (estimated)
Last update
Mar 1, 2023

Study contacts

Gloria Fernandez-Esparrach, PhD
Contact
mgfernan@clinic.cat
+34932275400
Rodrigo Garces-Duran, MD
Contact
rodrigogduran@hotmail.com
+34932275400
Gloria Fernandez-Esparrach, PhD
principal investigator · Hospital Clinic of Barcelona

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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