[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100648799":3},{"organization":4,"armGroups":7,"interventions":29,"overallOfficials":10,"centralContacts":59,"locations":68,"responsibleParty":109,"collaborators":10,"id":113,"slug":114,"hasResults":115,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":10,"eligibilityCriteria":119,"healthyVolunteers":115,"sex":120,"minAge":121,"maxAge":122,"enrollmentInfo":123,"targetDuration":10,"studyType":126,"phases":10,"briefSummary":127,"conditions":128,"keywords":131,"overallStatus":71,"whyStopped":10,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":155},{"fullName":5,"class":6},"Chinese PLA General Hospital","OTHER",[8,17,21,25],{"label":9,"type":10,"description":11,"interventionNames":12},"H. pylori-Positive Gastric Cancer Without Prior Eradication",null,"Participants 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\u002For 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.",[13,14,15,16],"Diagnostic Test: 13C-Urea Breath Test","Diagnostic Test: Serum Helicobacter pylori Antibody Testing","Diagnostic Test: Pathological Assessment of Gastric Tissue","Procedure: Endoscopic Submucosal Dissection",{"label":18,"type":10,"description":19,"interventionNames":20},"Persistent H. pylori-Positive Gastric Cancer After Eradication","Participants 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\u002For 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.",[13,14,15,16],{"label":22,"type":10,"description":23,"interventionNames":24},"H. pylori-Negative Gastric Cancer After Eradication","Participants 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.",[13,14,15,16],{"label":26,"type":10,"description":27,"interventionNames":28},"H. pylori-Negative Gastric Cancer With No Evidence of Infection","Participants 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.",[13,14,15,16],[30,38,45,52],{"type":31,"name":32,"description":33,"armGroupLabels":34,"otherNames":35},"DIAGNOSTIC_TEST","13C-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.",[22,26,9,18],[36,37],"13C-UBT","Urea Breath Test",{"type":31,"name":39,"description":40,"armGroupLabels":41,"otherNames":42},"Serum Helicobacter pylori Antibody Testing","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.",[22,26,9,18],[43,44],"H. pylori IgG Antibody Test","Serological Testing for H. pylori",{"type":31,"name":46,"description":47,"armGroupLabels":48,"otherNames":49},"Pathological Assessment of Gastric Tissue","Pathological assessment of gastric biopsy specimens and\u002For 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.",[22,26,9,18],[50,51],"Histopathological Assessment","Gastric Tissue Pathology",{"type":53,"name":54,"description":55,"armGroupLabels":56,"otherNames":57},"PROCEDURE","Endoscopic Submucosal Dissection","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.",[22,26,9,18],[58],"ESD",[60,65],{"name":61,"role":62,"phone":63,"phoneExt":10,"email":64},"He Zhou, PhD","CONTACT","+86-13029650138","zh505593673@163.com",{"name":66,"role":62,"phone":10,"phoneExt":10,"email":67},"Song Su, PhD","13439710906@163.com",[69,88,99],{"facility":70,"status":71,"city":72,"state":73,"zip":74,"country":75,"countryCode":76,"cosmosGeoPoint":77,"geoPoint":82,"contacts":83},"The Eighth Medical Center of Chinese PLA General Hospital","RECRUITING","Beijing","Beijing Municipality","100039","China","CN",{"type":78,"coordinates":79},"Point",[80,81],116.39723,39.9075,{"lat":81,"lon":80},[84],{"name":85,"role":62,"phone":86,"phoneExt":10,"email":87},"Shengzhen Liu","+86-128629079381","sz_liu@foxmail.com",{"facility":89,"status":71,"city":72,"state":73,"zip":90,"country":75,"countryCode":76,"cosmosGeoPoint":91,"geoPoint":93,"contacts":94},"First Medical Center of Chinese PLA General Hospital","100853",{"type":78,"coordinates":92},[80,81],{"lat":81,"lon":80},[95,96],{"name":61,"role":62,"phone":63,"phoneExt":10,"email":64},{"name":97,"role":62,"phone":98,"phoneExt":10,"email":67},"Song Su","+86-13439710906",{"facility":100,"status":71,"city":72,"state":73,"zip":10,"country":75,"countryCode":76,"cosmosGeoPoint":101,"geoPoint":103,"contacts":104},"Department of Gastroenterology, Rocket Force Characteristic Medical Center",{"type":78,"coordinates":102},[80,81],{"lat":81,"lon":80},[105],{"name":106,"role":62,"phone":107,"phoneExt":10,"email":108},"Jing Xie","+86-10-66343435","drxiejing@126.com",{"type":110,"investigatorFullName":111,"investigatorTitle":112,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","He Zhou","Professor","100648799","helicobacter-pylori-infection-status-and-pathological-features-for-predicting-gastric-cancer-biological-behavior-and-prognosis-a-real-world-observational-study-100648799",false,"NCT07724496","Helicobacter Pylori Infection Status and Pathological Features for Predicting Gastric Cancer Biological Behavior and Prognosis: A Real-World Observational Study","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","Inclusion Criteria:\n\n* Adults aged 18 to 80 years\n* 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\n* 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\n* Availability or planned availability of gastric tissue pathological assessment from routine biopsy specimens and\u002For endoscopic submucosal dissection specimens for evaluation of tissue-based H. pylori detection, background mucosal changes, lesion pathological characteristics, and ESD-related pathological findings\n* 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\n* 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\n* Adequate cardiac, hepatic, renal, and pulmonary function to tolerate endoscopic treatment and routine follow-up for prospectively enrolled participants scheduled for ESD\n* Ability to provide written informed consent for prospectively enrolled participants, or availability of ethics-approved retrospective clinical data for retrospectively included participants\n\nExclusion Criteria:\n\n* 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\n* 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\n* Lack of adequate pathological material or pathological information for assessment of gastric lesion characteristics, tissue-based H. pylori detection, or background mucosal changes\n* Previous gastrectomy or major gastric surgery that substantially alters gastric anatomy and prevents reliable assessment of lesion location, intragastric distribution, or background mucosal status\n* 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\n* 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\n* Pregnancy or breastfeeding for prospectively enrolled participants\n* Inability or unwillingness to comply with study procedures or follow-up requirements for prospectively enrolled participants\n* Any other condition judged by the investigators to make the participant unsuitable for the study","ALL","18 Years","80 Years",{"count":124,"type":125},1500,"ESTIMATED","OBSERVATIONAL","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).\n\nH. 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.\n\nThe 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.\n\nThe 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.\n\nFollow-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.",[129,130],"Helicobacter Pylori","Early Gastric Cancer",[132,130,54,58,32,133,134,135,136,137,138,139,140,141,142,143,144,145],"Helicobacter pylori","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","2026-07-20",{"date":148,"type":149},"2026-07-24","ACTUAL",{"date":151,"type":149},"2024-01-01",{"date":153,"type":125},"2031-12-30",{"name":5,"class":6},3]