[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100646892":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":10,"locations":10,"responsibleParty":12,"collaborators":10,"id":16,"slug":17,"hasResults":18,"nctId":19,"briefTitle":20,"officialTitle":20,"acronym":21,"eligibilityCriteria":22,"healthyVolunteers":18,"sex":23,"minAge":10,"maxAge":10,"enrollmentInfo":24,"targetDuration":10,"studyType":27,"phases":10,"briefSummary":28,"conditions":29,"keywords":10,"overallStatus":31,"whyStopped":10,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":10},{"fullName":5,"class":6},"Zhongshan Hospital Xiamen University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"The study plans to collect colorectal adenoma tissues from 30 patients initially detected by endosco",null,"The study plans to collect colorectal adenoma tissues from 30 patients initially detected by endoscopy, and perform scRNA-seq, scATAC-seq, and microbiome diversity sequencing on each sample, respectively. Two years after sampling, all enrolled patients will undergo follow-up colonoscopy; those found to have adenomas will be assigned to the recurrence group, while those without adenomas will be assigned to the non-recurrence group. By integrating multi-omics data for association analysis between the recurrence and non-recurrence groups, we aim to investigate the main driving factors of post-polypectomy recurrence, and to explore whether there exists an interpretable causal chain linking host epigenetic status, cellular transcriptional programs, and mucosa-associated microbiota that can explain recurrence risk and yield translatable biomarkers.",{"type":13,"investigatorFullName":14,"investigatorTitle":15,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Jianyin Zhou","Chief Physician","100646892","recurrence-mechanisms-of-colorectal-adenoma-after-resection-and-a-multi-omics-research-protocol-100646892",false,"NCT07683312","Recurrence Mechanisms of Colorectal Adenoma After Resection and a Multi-Omics Research Protocol","RM-CAR-MRP","Inclusion Criteria:\n\n* Patients with colorectal adenoma confirmed by initial endoscopic examination and pathological diagnosis.\n\nExclusion Criteria:\n\nUse of antibiotics within the past 2 weeks; Patients without colorectal adenoma; Patients with familial adenomatous polyposis; Patients with special dietary habits, such as vegetarians, alcoholics, binge eaters, or anorexic patients, etc.","ALL",{"count":25,"type":26},30,"ESTIMATED","OBSERVATIONAL","We aim to establish a single-cell atlas of primary adenomas, recurrent adenomas, and paired normal mucosa, identify recurrence-associated cell subpopulations and transcriptional pathways, and construct a risk prediction model for recurrence (integrating multi-omics features and clinical variables). Ultimately, we propose a panel of biomarkers that can be used to optimize follow-up strategies and guide potential microbiome-based interventions.\n\nUnder the premise of meeting routine clinicopathological requirements, we will collect tissue samples from 30 patients with colorectal adenomas. Each collected adenoma sample will be divided into three equal portions for scRNA-seq, scATAC-seq, and microbiome diversity sequencing, respectively. Two years after sampling, enrolled patients will undergo follow-up colonoscopy. Those in whom adenomas are detected will be classified as the recurrence group, while those without adenomas will be classified as the non-recurrence group. Sequencing data will be jointly analyzed in conjunction with clinical medical records. The tissue specimens obtained will not affect routine diagnosis or treatment outcomes.",[30],"Colorectal Adenoma and Carcinoma","NOT_YET_RECRUITING","2026-06-28",{"date":34,"type":35},"2026-07-06","ACTUAL",{"date":37,"type":26},"2026-06-27",{"date":39,"type":26},"2029-12-30",{"name":5,"class":6}]