Arrangement of Collecting Venules for the Endoscopic Diagnosis of Helicobacter Pylori

Helicobacter Pylori Infection Clinical Trial

— MOTIVATION  

Official title:

Arrangement of Collecting Venules for the Endoscopic Diagnosis of Helicobacter Pylori Infection (MOTIVATION): International Multicentre Study Outside Asia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05046990
• Other study ID #: HCB-RAC-MOTIVATION
• Status: Recruiting
• Start date: December 1, 2021
• Est. completion date: September 30, 2023

Study information

• Verified date: December 2022
• Source: Hospital Clinic of Barcelona
• Contact: Gloria Fernandez-Esparrach, PhD
• Phone: +34932275400
• Email: mgfernan[@]clinic.cat
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1000
• Est. completion date: September 30, 2023
• Est. primary completion date: June 30, 2023
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

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

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

Related Conditions & MeSH terms

• Helicobacter Infections
• Helicobacter Pylori Infection
• Infections

Intervention

Diagnostic Test:
• Regular Arrangement of Collecting Venules
This is a prospective, multicentre, international study without a control group.

Locations

Country	Name	City	State
Belgium	Cliniques Universitaires Saint Luc	Brussels
Germany	München University Hospital	Munich	Baviera
Spain	Hospital Clinic de Barcelona	Barcelona
Spain	Hospital de Mérida	Mérida	Badajoz
Spain	Hospital de Viladecans	Viladecans	Barcelona

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Clinic of Barcelona

Countries where clinical trial is conducted

Belgium,  Germany,  Spain, 

References & Publications (2)

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. — View Citation

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. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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).	12 months
Secondary	Baseline characteristics	To assess whether age, sex and PPIs, have an influence on the results of RAC in all patients.	12 months
Secondary	Histological correlation	To assess the correlation of atrophic gastritis and intestinal metaplasia (confirmed in histopathological samples) and RAC in all patients.	12 months
Secondary	Reproducibility	To assess reproducibility of RAC on real time examinations with different operators and in different countries with different Hp infection prevalence.	12 months