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Helicobacter PyloriNCT07724496

Helicobacter Pylori Infection Status and Pathological Features for Predicting Gastric Cancer Biological Behavior and Prognosis: A Real-World Observational Study

An observational study of Helicobacter Pylori and Early Gastric Cancer, run by Chinese PLA General Hospital at 3 sites in China.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This multicenter retrospective and prospective real-world observational study will evaluate the relationship of Helicobacter pylori (H. pylori) infection status, intragastric distribution, and pathological features with gastric cancer biological behavior and long-term prognosis in patients with early gastric cancer or… Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Helicobacter Pylori, Early Gastric Cancer
What is being tested?
13C-Urea Breath Test, Serum Helicobacter pylori Antibody Testing and Pathological Assessment of Gastric Tissue
Type of treatment
Surgery or procedure
How many people
1,500 participants
Where
3 sitesChina
Study dates
1 Jan 2024to 30 Dec 2031
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adults aged 18 to 80 years with early gastric cancer, high-grade intraepithelial neoplasia, or other gastric neoplastic lesions treated with or scheduled for endoscopic submucosal dissection at participating medical centers. The study will include approximately 1000 retrospectively identified participants with available clinical, endoscopic, pathological, H. pylori testing, and follow-up records, and approximately 500 prospectively enrolled participants. H. pylori infection and eradication status, tissue-based and intragastric H. pylori distribution, pathological features, gastric cancer subtype, biological behavior, ESD curability, and outcomes at 1, 2, and 3 years after ESD and during long-term follow-up will be evaluated.

Who may be able to join

  • Adults aged 18 to 80 years
  • Retrospectively identified or prospectively enrolled patients with early gastric cancer, high-grade intraepithelial neoplasia, or other gastric neoplastic lesions treated with or scheduled for endoscopic submucosal dissection according to standard clinical indications at participating medical centers
  • Availability or planned availability of sufficient Helicobacter pylori assessment data for study classification, including 13C-urea breath test, serum Helicobacter pylori IgG antibody testing, pathological assessment of gastric tissue, prior H. pylori infection history, prior eradication history, eradication confirmation, or follow-up H. pylori testing results when available
  • Availability or planned availability of gastric tissue pathological assessment from routine biopsy specimens and/or endoscopic submucosal dissection specimens for evaluation of tissue-based H. pylori detection, background mucosal changes, lesion pathological characteristics, and ESD-related pathological findings
  • Availability or planned availability of key clinical, endoscopic, and pathological information required to evaluate gastric cancer subtype, biological behavior, and curability after ESD, including lesion location, histological subtype, differentiation, depth of invasion, lymphovascular invasion, margin status, curative resection status, and additional treatment information when available
  • Availability of follow-up data for retrospectively included participants, or willingness and ability to participate in follow-up evaluations for prospectively enrolled participants, including endoscopic follow-up at approximately 1, 2, and 3 years after ESD and longer-term follow-up when available
  • Adequate cardiac, hepatic, renal, and pulmonary function to tolerate endoscopic treatment and routine follow-up for prospectively enrolled participants scheduled for ESD
  • Ability to provide written informed consent for prospectively enrolled participants, or availability of ethics-approved retrospective clinical data for retrospectively included participants

Who cannot join

  • Patients whose final diagnosis does not meet the study population definition, including those without early gastric cancer, high-grade intraepithelial neoplasia, or other eligible gastric neoplastic lesions
  • Insufficient clinical, H. pylori testing, endoscopic, pathological, or follow-up information to classify H. pylori infection or eradication status or to evaluate the main study outcomes
  • Lack of adequate pathological material or pathological information for assessment of gastric lesion characteristics, tissue-based H. pylori detection, or background mucosal changes
  • Previous gastrectomy or major gastric surgery that substantially alters gastric anatomy and prevents reliable assessment of lesion location, intragastric distribution, or background mucosal status
  • For prospectively enrolled participants scheduled for ESD, severe comorbid conditions, such as uncontrolled cardiovascular or cerebrovascular disease, severe coagulopathy, or very poor general condition, that make endoscopic submucosal dissection unsafe
  • For prospectively enrolled participants scheduled for ESD, anticoagulant or antiplatelet therapy that cannot be safely interrupted or managed during the perioperative period, or active bleeding tendency judged to significantly increase procedural risk
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  • Pregnancy or breastfeeding for prospectively enrolled participants
  • Inability or unwillingness to comply with study procedures or follow-up requirements for prospectively enrolled participants
  • Any other condition judged by the investigators to make the participant unsuitable for the study

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Song Su, PhD contact

13439710906@163.com

China3 sites, 3 recruiting
  • The Eighth Medical Center of Chinese PLA General Hospital

    Beijing, Beijing Municipality, 100039

    Shengzhen Liu, +86-128629079381, sz_liu@foxmail.com

    Recruiting
  • First Medical Center of Chinese PLA General Hospital

    Beijing, Beijing Municipality, 100853

    He Zhou, PhD, +86-13029650138, zh505593673@163.com

    Song Su, +86-13439710906, 13439710906@163.com

    Recruiting
  • Department of Gastroenterology, Rocket Force Characteristic Medical Center

    Beijing, Beijing Municipality

    Jing Xie, +86-10-66343435, drxiejing@126.com

    Recruiting

Other trials in China

About this study

Official title: A Multicenter Retrospective and Prospective Real-World Observational Study of Helicobacter Pylori Infection Status and Pathological Features of Early Gastric Cancer for Predicting Biological Behavior and Prognosis Across Gastric Cancer Subtypes

This multicenter retrospective and prospective real-world observational study will evaluate the relationship of Helicobacter pylori (H. pylori) infection status, intragastric distribution, and pathological features with gastric cancer biological behavior and long-term prognosis in patients with early gastric cancer or related gastric neoplastic lesions undergoing endoscopic submucosal dissection (ESD).

  1. pylori infection is an important risk factor for gastric cancer. In clinical practice, H. pylori status can be assessed by several methods, including the 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue. These methods may not always provide the same result because they reflect different aspects of infection, including current active infection, previous exposure, prior eradication status, and local tissue-based detection.
Read more

The study will include approximately 1500 participants from participating medical centers. About 1000 participants will be retrospectively identified from existing clinical, endoscopic, pathological, H. pylori testing, and follow-up records, and about 500 additional participants will be prospectively enrolled.

The study will evaluate H. pylori infection status, prior eradication status, discordant testing patterns, tissue-based and intragastric H. pylori distribution, background mucosal changes, and pathological features of early gastric cancer or related gastric neoplastic lesions. These features will be analyzed in relation to different gastric cancer subtypes and biological behavior.

Follow-up information will be used to evaluate whether the integrated analysis of H. pylori infection status and pathological features can predict clinical outcomes at 1, 2, and 3 years after ESD and during long-term follow-up, including local recurrence, metachronous gastric cancer, synchronous or multifocal early gastric cancer detected within 1 year, additional surgical treatment, survival, and other clinically meaningful outcomes.

Read the detailed description

Background and Rationale:

Helicobacter pylori (H. pylori) infection is a major risk factor for gastric cancer and is closely associated with chronic gastritis, mucosal atrophy, intestinal metaplasia, dysplasia, and gastric carcinogenesis. Although H. pylori eradication can reduce the risk of gastric cancer, some patients still develop gastric cancer after eradication therapy, and patients treated with endoscopic submucosal dissection (ESD) may remain at risk for local recurrence, metachronous gastric cancer, and other gastric neoplastic lesions during follow-up.

In clinical practice, H. pylori status can be evaluated by several methods, including the 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue. These methods reflect different biological and clinical information. The 13C-urea breath test mainly reflects current active infection, serum antibody testing may reflect previous or current exposure, and pathological assessment provides local tissue-based information from specific gastric sites.

However, these test results may be inconsistent. H. pylori colonization can be patchy and unevenly distributed within the stomach. In patients with early gastric cancer, local tumor-related changes, mucosal atrophy, intestinal metaplasia, spasmolytic polypeptide-expressing metaplasia, prior eradication therapy, and changes in the gastric mucosal microenvironment may influence bacterial density and detectability. Therefore, a negative pathological finding in the tumor area does not necessarily exclude previous H. pylori exposure or H. pylori-related background mucosal changes.

Current evidence suggests that H. pylori may be more frequently detected in non-tumor or peritumoral mucosa than in tumor tissue itself, and that H. pylori-related mucosal changes may be associated with specific pathological phenotypes of early gastric cancer. Nevertheless, the clinical meaning of discordant H. pylori test patterns and the relationship among H. pylori intragastric distribution, gastric pathological characteristics, post-eradication gastric cancer, and metachronous gastric cancer remain insufficiently understood.

Study Objective:

The overall objective of this study is to establish a sequential clinical-pathological framework linking Helicobacter pylori (H. pylori) test heterogeneity, pathological features including tissue-based and intragastric H. pylori distribution, gastric cancer subtype and biological behavior, and long-term prognosis in patients with early gastric cancer or related gastric neoplastic lesions undergoing endoscopic submucosal dissection (ESD).

The study will focus on four linked components:

  1. To characterize heterogeneity among different H. pylori testing results, including 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue. Concordant and discordant testing patterns will be used to define current infection, previous exposure, post-eradication status, no evidence of infection, and tissue-based H. pylori detection.
  2. To evaluate pathological features associated with these H. pylori testing patterns, including tissue-based and intragastric H. pylori distribution in tumor tissue, lesion-adjacent mucosa, and non-lesion background mucosa when available. Background mucosal changes, including chronic inflammation, active inflammation, atrophy, intestinal metaplasia, dysplasia, and other pathology-reported mucosal findings, will also be assessed. Lesion-level pathological features, including lesion location, histological subtype, differentiation, depth of invasion, lymphovascular invasion, and margin status, will be recorded.
  3. To classify and compare different gastric cancer subtypes and biological behavior patterns according to the preceding H. pylori testing and pathological features. These subtypes may include current or persistent H. pylori infection-associated gastric cancer, past exposure or post-eradication gastric cancer, gastric cancer with no evidence of H. pylori infection, proximal versus distal gastric cancer, differentiated versus undifferentiated histology, and solitary versus synchronous or multifocal early gastric cancer detected within 1 year when applicable.
  4. To evaluate long-term clinical outcomes after ESD, with particular attention to whether the integrated analysis of H. pylori infection status and pathological features can predict long-term outcomes in early gastric cancer, including local recurrence, metachronous gastric cancer, additional surgical treatment, survival, and other clinically meaningful outcomes.

Study Design:

This is a multicenter retrospective and prospective real-world observational cohort study led by Chinese PLA General Hospital and conducted at participating medical centers. Approximately 1500 participants will be included. About 1000 participants will be retrospectively identified from existing clinical records, endoscopic databases, H. pylori testing records, ESD pathological records, and follow-up information. About 500 additional participants are planned to be prospectively enrolled.

Eligible participants will be patients with early gastric cancer, high-grade intraepithelial neoplasia, or other gastric neoplastic lesions treated with or scheduled for ESD according to standard clinical indications.

This study is observational. Participants will not be assigned to any experimental intervention by the study protocol. All diagnostic evaluation, H. pylori testing, ESD treatment, perioperative management, pathological assessment, H. pylori eradication therapy when clinically indicated, and follow-up will be performed according to routine clinical practice and institutional standards.

  1. pylori Assessment:

For retrospectively included participants, available H. pylori testing results will be extracted from existing medical records, including 13C-urea breath test, serum H. pylori antibody testing, pathological assessment, prior eradication history, eradication confirmation, and follow-up H. pylori testing results when available.

For prospectively enrolled participants, H. pylori assessment will be performed according to routine clinical practice, including serum H. pylori IgG antibody testing and the 13C-urea breath test before ESD when clinically indicated. Pathological assessment of gastric tissue will be collected from routine clinical specimens when available, including diagnostic biopsy specimens and ESD specimens.

Participants will be categorized according to H. pylori infection and eradication patterns, including H. pylori-positive gastric cancer without prior eradication, persistent H. pylori-positive gastric cancer after eradication, H. pylori-negative gastric cancer after eradication, and H. pylori-negative gastric cancer with no evidence of infection.

Intragastric Distribution and Background Mucosal Assessment:

The study will record the anatomical location of gastric lesions and available tissue-based findings by gastric region. Locations may include the cardia, fundus, gastric body, gastric angle, and antrum, as well as lesser curvature, greater curvature, anterior wall, and posterior wall when available.

When tissue material allows, pathological assessment will evaluate H. pylori detection in tumor tissue, lesion-adjacent mucosa, and non-lesion background mucosa. Background mucosal changes, including chronic inflammation, active inflammation, atrophy, intestinal metaplasia, and other pathology-reported mucosal findings, will be recorded when available. These findings will be used to explore whether discordant H. pylori test patterns can be explained by intragastric distribution, local tissue detectability, or background mucosal changes.

Endoscopic and Pathological Assessment:

Endoscopic data will include lesion location, lesion size, macroscopic morphology, surface characteristics, ulceration or scar findings, and other relevant endoscopic features.

Pathological data will include histological diagnosis, histological subtype, degree of differentiation, depth of invasion, lymphovascular invasion, horizontal and vertical margin status, and whether curative resection criteria are met when applicable. The study will evaluate whether H. pylori infection status, prior eradication status, discordant testing patterns, and intragastric distribution are associated with gastric cancer pathological features and background mucosal changes.

Perioperative Outcomes:

Although the main focus of this study is H. pylori status, intragastric distribution, pathological characteristics, and long-term prognosis, ESD-related perioperative outcomes will also be collected as clinically relevant supportive data. These may include intraoperative bleeding requiring endoscopic hemostasis, procedure duration, intraoperative perforation, en bloc resection, R0 resection, delayed bleeding, postoperative complications, and length of hospital stay.

Long-term Follow-up:

Participants will be followed after ESD according to routine clinical practice. For retrospectively included participants, available follow-up information at approximately 1, 2, and 3 years after ESD and longer-term follow-up when available will be extracted from medical records, endoscopic follow-up records, pathological reports, telephone follow-up, and survival information. For prospectively enrolled participants, follow-up will be conducted according to routine clinical practice.

Follow-up evaluations may include outpatient visits, telephone follow-up, endoscopic examination, imaging examination when clinically indicated, and review of medical records. Follow-up outcomes will be assessed at 1, 2, and 3 years after ESD and during long-term follow-up through study completion. Outcomes will include local residual disease, local recurrence, synchronous or multifocal early gastric cancer detected within 1 year, metachronous gastric cancer, additional surgical treatment, survival status, and other clinically relevant outcomes.

Follow-up endoscopy will usually be performed every 6 to 12 months according to clinical practice and individual risk. H. pylori eradication therapy, when clinically indicated, will be recorded, as will subsequent changes in H. pylori status when follow-up testing is available.

Analysis Plan:

The study will first summarize H. pylori test patterns based on 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment. Concordance and discordance among these testing modalities will be evaluated using overall agreement rates, pairwise agreement rates, and agreement statistics when appropriate.

The study will then describe H. pylori intragastric and tissue-based distribution and related background mucosal changes by gastric region and pathological compartment. Associations between H. pylori test patterns, prior eradication status, tissue distribution, background mucosal changes, and gastric pathological features will be evaluated using appropriate statistical methods. Categorical variables will be compared using chi-square or Fisher's exact tests, and continuous variables will be compared using parametric or non-parametric tests depending on distribution.

For long-term outcomes, local recurrence, metachronous gastric cancer, additional surgical treatment, recurrence-free survival, overall survival, and other clinically meaningful outcomes will be assessed at 1, 2, and 3 years after ESD and during long-term follow-up through study completion. Logistic regression or Cox proportional hazards models may be used to identify factors associated with these outcomes when sufficient events are available. Potential covariates may include age, sex, study center, retrospective versus prospective data source, lesion location, lesion size, histological type, differentiation, depth of invasion, lymphovascular invasion, margin status, atrophy or intestinal metaplasia, H. pylori testing pattern, tissue-based H. pylori distribution, and prior eradication history.

Study Significance:

This study is intended to provide a systematic clinical and pathological evaluation of H. pylori infection status, discordant test patterns, tissue-based and intragastric distribution, pathological features, gastric cancer biological behavior, and long-term outcomes in patients undergoing ESD for early gastric cancer or related gastric neoplastic lesions.

The findings may help improve interpretation of H. pylori test results, clarify the pathological basis of discordant H. pylori detection, and identify H. pylori-related background mucosal changes. In addition, this study aims to characterize the pathological features and biological behavior of gastric cancer after H. pylori eradication and other H. pylori-related gastric cancer subtypes.

By integrating H. pylori infection status, prior eradication status, tissue-based H. pylori distribution, background mucosal changes, and tumor pathological characteristics, this study may support subtype-specific prognostic evaluation and risk-adapted surveillance strategies for local recurrence, metachronous gastric cancer, additional surgical treatment, and other clinically meaningful outcomes after ESD.

Being tested
13C-Urea Breath Test, Serum Helicobacter pylori Antibody Testing, Pathological Assessment of Gastric Tissue, Endoscopic Submucosal Dissection
Keywords
Helicobacter pylori, Early Gastric Cancer, Endoscopic Submucosal Dissection, ESD, 13C-Urea Breath Test, Serum Helicobacter pylori Antibody, Intragastric Distribution, Gastric Cancer Pathology, H. pylori Eradication, Post-eradication Gastric Cancer, Pathological Assessment, H. pylori Test Concordance, Discordant H. pylori Testing, Background Mucosal Changes, Gastric Mucosal Atrophy, Intestinal Metaplasia, Metachronous Gastric Cancer, Long-Term Outcomes
Medical subject headings
Stomach Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 13C-Urea Breath TestDiagnostic test

    Also called 13C-UBT, Urea Breath Test

    The 13C-urea breath test is performed before endoscopic submucosal dissection as part of routine clinical evaluation to assess current active Helicobacter pylori infection. The result will be compared with serum Helicobacter pylori antibody testing and pathological assessment to evaluate diagnostic concordance. This test is not assigned as an experimental intervention by the study protocol.

  • Serum Helicobacter pylori Antibody TestingDiagnostic test

    Also called H. pylori IgG Antibody Test, Serological Testing for H. pylori

    Serum Helicobacter pylori antibody testing is performed before endoscopic submucosal dissection as part of routine clinical evaluation to assess previous or current exposure to H. pylori. The result will be compared with the 13C-urea breath test and pathological assessment to evaluate diagnostic concordance and discordant H. pylori testing patterns.

  • Pathological Assessment of Gastric TissueDiagnostic test

    Also called Histopathological Assessment, Gastric Tissue Pathology

    Pathological assessment of gastric biopsy specimens and/or endoscopic submucosal dissection specimens will be performed as part of routine clinical care. Tissue-based findings will be used to evaluate H. pylori detection in tumor tissue, lesion-adjacent mucosa, and non-lesion background mucosa when available. Background mucosal changes such as chronic inflammation, active inflammation, atrophy, intestinal metaplasia, and other pathology-reported findings will be recorded. Gastric cancer pathological features, including histology, differentiation, invasion depth, lymphovascular invasion, and margin status, will also be assessed.

  • Endoscopic Submucosal DissectionProcedure or surgery

    Also called ESD

    Endoscopic submucosal dissection is performed as standard clinical treatment for eligible early gastric cancer or related gastric neoplastic lesions. The procedure is not assigned by the study protocol. ESD-related procedural data, resection quality, postoperative outcomes, pathological findings, recurrence, metachronous gastric cancer, and long-term prognosis will be collected for observational analysis.

Study groups in NCT07724496
Study groupRoleWhat they receive
H. pylori-Positive Gastric Cancer Without Prior EradicationParticipants with early gastric cancer or related gastric neoplastic lesions who have evidence of current active Helicobacter pylori infection before endoscopic submucosal dissection and no documented history of prior H. pylori eradication therapy. Current active infection is primarily defined by a positive 13C-urea breath test and/or positive tissue-based pathological detection of H. pylori before or at the time of ESD. Serum H. pylori antibody status, pathological features, tissue-based H. pylori distribution, and long-term outcomes will be recorded and analyzed.
Receives: Diagnostic Test: 13C-Urea Breath Test; Diagnostic Test: Serum Helicobacter pylori Antibody Testing; Diagnostic Test: Pathological Assessment of Gastric Tissue; Procedure: Endoscopic Submucosal Dissection
Persistent H. pylori-Positive Gastric Cancer After EradicationParticipants with early gastric cancer or related gastric neoplastic lesions who have a documented history of H. pylori eradication therapy before endoscopic submucosal dissection but still show evidence of persistent or recurrent active H. pylori infection at baseline. Persistent positivity may be defined by a positive 13C-urea breath test and/or positive tissue-based pathological detection of H. pylori after prior eradication therapy. This cohort will be used to evaluate pathological features, tissue-based and intragastric H. pylori distribution, biological behavior, and long-term outcomes in gastric cancer associated with eradication failure or persistent infection.
Receives: Diagnostic Test: 13C-Urea Breath Test; Diagnostic Test: Serum Helicobacter pylori Antibody Testing; Diagnostic Test: Pathological Assessment of Gastric Tissue; Procedure: Endoscopic Submucosal Dissection
H. pylori-Negative Gastric Cancer After EradicationParticipants with early gastric cancer or related gastric neoplastic lesions who have a documented history of H. pylori eradication therapy before endoscopic submucosal dissection and no evidence of current active infection at baseline. Absence of current active infection is primarily defined by a negative 13C-urea breath test, with tissue-based pathological assessment recorded when available. Serum H. pylori antibody may remain positive or weakly positive because of previous exposure. This cohort will be used to evaluate the pathological features, biological behavior, background mucosal changes, and long-term outcomes of post-eradication gastric cancer.
Receives: Diagnostic Test: 13C-Urea Breath Test; Diagnostic Test: Serum Helicobacter pylori Antibody Testing; Diagnostic Test: Pathological Assessment of Gastric Tissue; Procedure: Endoscopic Submucosal Dissection
H. pylori-Negative Gastric Cancer With No Evidence of InfectionParticipants with early gastric cancer or related gastric neoplastic lesions who have no documented history of H. pylori infection or eradication therapy and no evidence of H. pylori infection at baseline. This cohort is defined by negative serum H. pylori antibody testing, negative 13C-urea breath test, and no tissue-based pathological detection of H. pylori when pathological information is available. Pathological features, background mucosal changes, gastric cancer subtype, biological behavior, and long-term outcomes will be recorded and compared with the other cohorts.
Receives: Diagnostic Test: 13C-Urea Breath Test; Diagnostic Test: Serum Helicobacter pylori Antibody Testing; Diagnostic Test: Pathological Assessment of Gastric Tissue; Procedure: Endoscopic Submucosal Dissection

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Concordance Rate Among Three H. pylori Testing Modalities in Post-Eradication Gastric Cancer

    The concordance rate among three H. pylori testing modalities will be reported in participants with post-eradication gastric cancer. The three testing modalities include 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue. Each test result will be classified as positive or negative according to the corresponding clinical laboratory or pathology report. Concordance is defined as all three testing modalities yielding the same binary result, either all positive or all negative. The unit of measure is the percentage of participants with concordant results among participants with available results from all three testing modalities.

    Measured: From baseline H. pylori testing to pathological assessment within 2 weeks after endoscopic submucosal dissection

Secondary outcomes (19)
  1. Positive Detection Rate of Serum H. pylori Antibody Testing in Post-Eradication Gastric Cancer

    The positive detection rate of serum H. pylori antibody testing will be reported in participants with post-eradication gastric cancer. The unit of measure is the percentage of participants with a positive or weakly positive serum H. pylori antibody result among participants with available test results.

    Measured: Baseline

  2. Positive Detection Rate of Pathological H. pylori Assessment in Post-Eradication Gastric Cancer

    The positive detection rate of pathological H. pylori assessment will be reported in participants with post-eradication gastric cancer. The unit of measure is the percentage of participants with H. pylori detected by pathological assessment of gastric biopsy or endoscopic submucosal dissection specimens among participants with available pathological results.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  3. Discordance Rate Among Three H. pylori Testing Modalities in Post-Eradication Gastric Cancer

    The discordance rate among three H. pylori testing modalities will be reported in participants with post-eradication gastric cancer. Discordance is defined as inconsistent binary results among 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue. The unit of measure is the percentage of participants with discordant results among participants with available results from all three testing modalities.

    Measured: From baseline H. pylori testing to pathological assessment within 2 weeks after endoscopic submucosal dissection

  4. Kappa Coefficient for Agreement Among Three H. pylori Testing Modalities

    The kappa coefficient for agreement among 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment of gastric tissue will be calculated when sufficient data are available.

    Measured: From baseline H. pylori testing to pathological assessment within 2 weeks after endoscopic submucosal dissection

  5. Percentage of Participants With Tissue-Based H. pylori Detection in Tumor Tissue

    The percentage of participants with H. pylori detected in tumor tissue will be reported among participants with available pathological assessment of tumor tissue. H. pylori detection will be assessed by routine pathological examination, special staining, or immunohistochemistry when available.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  6. Percentage of Participants With Tissue-Based H. pylori Detection in Lesion-Adjacent Mucosa

    The percentage of participants with H. pylori detected in lesion-adjacent gastric mucosa will be reported among participants with available pathological assessment of lesion-adjacent mucosa. H. pylori detection will be assessed by routine pathological examination, special staining, or immunohistochemistry when available.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  7. Percentage of Participants With Tissue-Based H. pylori Detection in Non-Lesion Background Mucosa

    The percentage of participants with H. pylori detected in non-lesion background gastric mucosa will be reported among participants with available pathological assessment of background mucosa. H. pylori detection will be assessed by routine pathological examination, special staining, or immunohistochemistry when available.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  8. Percentage of Participants With Background Gastric Mucosal Atrophy

    The percentage of participants with gastric mucosal atrophy in available biopsy or endoscopic submucosal dissection specimens will be reported. Gastric mucosal atrophy will be assessed by routine pathological examination.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  9. Percentage of Participants With Background Intestinal Metaplasia

    The percentage of participants with intestinal metaplasia in available biopsy or endoscopic submucosal dissection specimens will be reported. Intestinal metaplasia will be assessed by routine pathological examination.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  10. Percentage of Participants in Each H. pylori-Defined Gastric Cancer Subtype

    The percentage of participants in each H. pylori-defined gastric cancer subtype will be reported. Subtypes include H. pylori-positive gastric cancer without prior eradication, persistent H. pylori-positive gastric cancer after eradication, H. pylori-negative gastric cancer after eradication, and H. pylori-negative gastric cancer with no evidence of infection. Classification will be based on prior eradication history, 13C-urea breath test, serum H. pylori antibody testing, and pathological assessment when available.

    Measured: Baseline to pathological assessment within 2 weeks after endoscopic submucosal dissection

  11. Percentage of Participants With Synchronous or Multifocal Early Gastric Cancer Within 1 Year

    The percentage of participants with synchronous or multifocal early gastric cancer or high-grade intraepithelial neoplasia detected at baseline or within 1 year after endoscopic submucosal dissection will be reported. Events will be identified by endoscopy and confirmed by pathological assessment.

    Measured: The percentage of participants with synchronous or multifocal early gastric cancer or high-grade intraepithelial neoplasia detected at baseline or within 1 year after endoscopic submucosal dissection will be reported. Events will be identified by endosco

  12. Cumulative Incidence of Metachronous Gastric Cancer After Endoscopic Submucosal Dissection

    The cumulative incidence of metachronous gastric cancer after endoscopic submucosal dissection will be reported. Metachronous gastric cancer is defined as newly detected gastric cancer at a site different from the original endoscopic submucosal dissection lesion, identified by follow-up endoscopy and confirmed by pathological assessment. Local residual disease or local recurrence at the original endoscopic submucosal dissection site will not be counted as metachronous gastric cancer.

    Measured: 1 year, 2 years, 3 years, and through study completion, up to 8 years after endoscopic submucosal dissection

  13. Percentage of Participants With Local Residual or Recurrent Gastric Neoplasia

    The percentage of participants with local residual or recurrent gastric neoplasia at or near the original endoscopic submucosal dissection site will be reported. Events will be identified by follow-up endoscopy and confirmed by pathological assessment or clinical records.

    Measured: 1 year, 2 years, and 3 years after endoscopic submucosal dissection

  14. Percentage of Participants Requiring Additional Surgical Treatment After Endoscopic Submucosal Dissection

    The percentage of participants requiring additional surgical treatment after endoscopic submucosal dissection will be reported. Additional surgery may be performed because of non-curative resection, high-risk pathological features, residual or recurrent disease, metachronous gastric neoplasia, or other clinically indicated reasons.

    Measured: 1 year, 2 years, and 3 years after endoscopic submucosal dissection

  15. Recurrence-Free Survival After Endoscopic Submucosal Dissection

    Recurrence-free survival will be defined as the time from endoscopic submucosal dissection to the first occurrence of local residual disease, local recurrence, metachronous gastric cancer, gastric neoplastic recurrence, or death from any cause.

    Measured: From endoscopic submucosal dissection to 3 years after endoscopic submucosal dissection

  16. Overall Survival After Endoscopic Submucosal Dissection

    Overall survival will be defined as the time from endoscopic submucosal dissection to death from any cause.

    Measured: From endoscopic submucosal dissection to 3 years after endoscopic submucosal dissection

  17. Distribution of SMIS-Cure Curability Grades After Endoscopic Submucosal Dissection

    The percentage of participants in each SMIS-Cure curability grade after endoscopic submucosal dissection will be reported. SMIS-Cure grades include Grade A, Grade B, and Grade C, based on available clinical, endoscopic, imaging, and pathological information.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  18. Distribution of eCure Classifications After Endoscopic Submucosal Dissection

    The percentage of participants in each eCure classification after endoscopic submucosal dissection will be reported. The eCure system evaluates curability and lymph node metastasis risk after endoscopic resection based on post-ESD pathological factors, including tumor size, vertical margin status, lymphatic invasion, venous invasion, and depth of invasion.

    Measured: Within 2 weeks after endoscopic submucosal dissection

  19. Kappa Coefficient for Agreement Between SMIS-Cure and eCure Classifications

    The kappa coefficient for agreement between SMIS-Cure curability grades and eCure classifications will be calculated when sufficient data are available.

    Measured: Within 2 weeks after endoscopic submucosal dissection

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jul 2026
  2. Study start1 Jan 2024
  3. Primary completion30 Dec 2031 (estimated)
  4. Study completion30 Dec 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07724496
Sponsor's protocol ID
S2024-268-01
Status last verified
Jul 2026
First submitted
16 Jun 2026
Last updated
24 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Oda I, Suzuki H, Nonaka S, Yoshinaga S. Complications of gastric endoscopic submucosal dissection. Dig Endosc. 2013 Mar;25 Suppl 1:71-8. doi: 10.1111/j.1443-1661.2012.01376.x. Epub 2013 Jan 24.

    PubMed 23368986
  • Polk DB, Peek RM Jr. Helicobacter pylori: gastric cancer and beyond. Nat Rev Cancer. 2010 Jun;10(6):403-14. doi: 10.1038/nrc2857.

    PubMed 20495574

Questions about this trial

What is this clinical trial studying?

An observational study of Helicobacter Pylori and Early Gastric Cancer, run by Chinese PLA General Hospital at 3 sites in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 24 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact He Zhou, PhD (+86-13029650138, zh505593673@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Concordance Rate Among Three H. pylori Testing Modalities in Post-Eradication Gastric Cancer (time frame: From baseline H. pylori testing to pathological assessment within 2 weeks after endoscopic submucosal dissection). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07724496, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jul 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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