[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621125":3},{"organization":4,"outcomesModule":7,"designInfo":34,"detailedDescription":37,"studyPopulation":38,"armGroups":39,"interventions":33,"overallOfficials":33,"centralContacts":43,"locations":49,"responsibleParty":65,"collaborators":33,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":33,"eligibilityCriteria":74,"healthyVolunteers":70,"sex":75,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":81,"studyType":82,"phases":33,"briefSummary":83,"conditions":84,"keywords":87,"overallStatus":99,"whyStopped":33,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"Bundang CHA Hospital","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":19,"otherOutcomes":33},[9,13,15,17],{"measure":10,"description":11,"timeFrame":12},"Methylation index of SFRP2 in colorectal tissue","Quantitative assessment of DNA methylation levels in adenomatous versus adjacent normal colorectal tissues. Methylation levels will be determined using quantitative methylation-specific PCR (qMSP) and expressed as methylation index (MtI, %).","Baseline (Single Time Point)]",{"measure":14,"description":11,"timeFrame":12},"Methylation index of TFPI2 in colorectal tissue",{"measure":16,"description":11,"timeFrame":12},"Methylation index of SEPT9 in colorectal tissue",{"measure":18,"description":11,"timeFrame":12},"Methylation index of SDC2 in colorectal tissue",[20,24,27,30],{"measure":21,"description":22,"timeFrame":23},"Sensitivity and specificity of methylated SFRP2 for detecting adenoma","Receiver operating characteristic (ROC) curve analysis will be used to evaluate the diagnostic performance of methylated SFRP2 in distinguishing adenomatous from normal tissue. The percentage of methylated reference (PMR) values derived from qMSP will be compared between groups.","Baseline (Single Time Point)",{"measure":25,"description":26,"timeFrame":23},"Sensitivity and specificity of methylated TFPI2 for detecting adenoma","Receiver operating characteristic (ROC) curve analysis will be used to evaluate the diagnostic performance of methylated TFPI2 in distinguishing adenomatous from normal tissue. The percentage of methylated reference (PMR) values derived from qMSP will be compared between groups.",{"measure":28,"description":29,"timeFrame":23},"Sensitivity and specificity of methylated SEPT9 for detecting adenoma","Receiver operating characteristic (ROC) curve analysis will be used to evaluate the diagnostic performance of methylated SEPT9 in distinguishing adenomatous from normal tissue. The percentage of methylated reference (PMR) values derived from qMSP will be compared between groups.",{"measure":31,"description":32,"timeFrame":23},"Sensitivity and specificity of methylated SDC2 for detecting adenoma","Receiver operating characteristic (ROC) curve analysis will be used to evaluate the diagnostic performance of methylated SDC2 in distinguishing adenomatous from normal tissue. The percentage of methylated reference (PMR) values derived from qMSP will be compared between groups.",null,{"allocation":33,"interventionModel":33,"interventionModelDescription":33,"primaryPurpose":33,"observationalModel":35,"timePerspective":36,"maskingInfo":33},"CASE_CONTROL","CROSS_SECTIONAL","Colorectal cancer (CRC) is one of the most common malignancies in Korea, ranking second in national cancer incidence statistics. Most CRCs arise through the adenoma-carcinoma sequence, in which epigenetic and genetic alterations play critical roles. Identifying methylated genetic markers in colorectal adenoma may provide insights into early carcinogenic mechanisms and enable more individualized surveillance strategies after polypectomy.\n\nThis study focuses on exploring epigenetic factors-particularly DNA methylation patterns-associated with colorectal adenoma in Korean patients. A total of 32 participants undergoing colonoscopic polypectomy will be recruited. From each participant, both adenomatous tissue and adjacent normal mucosa (approximately 5 millimeters (mm) in size) will be collected. Stool samples will also be obtained for microbiome and genomic analysis.\n\nDNA extracted from tissue and stool samples will undergo bisulfite conversion using the EZ DNA Methylation-Gold Kit (Zymo Research). Quantitative methylation-specific polymerase chain reaction (qMSP) will be performed to evaluate promoter methylation levels of four candidate genes-SFRP2 (Secreted Frizzled Related Protein 2), TFPI2 (Tissue Factor Pathway Inhibitor 2), SEPT9 (Septin 9), and SDC2 (Syndecan 2)-that have previously shown potential as colorectal neoplasia biomarkers. Selected samples will also undergo Sanger sequencing for CpG-level methylation profiling. Stool DNA will be analyzed through whole-genome sequencing (WGS) on the Illumina NovaSeq 6000 platform to assess microbial composition and genetic context.\n\nMethylation indices (MtI) and percentage of methylated reference (PMR) values will be calculated and compared between adenoma and adjacent normal tissues. Receiver operating characteristic (ROC) curve analysis will determine the sensitivity and specificity of each gene as a potential biomarker.\n\nBy identifying methylated genes that are significantly upregulated in adenomatous tissues, this study aims to propose candidate epigenetic markers for predicting the recurrence or malignant transformation of colorectal adenoma. The findings may contribute to refining post-polypectomy surveillance intervals and supporting precision prevention strategies in CRC.","Patients undergoing colonoscopic polypectomy for colorectal adenoma at Bundang CHA Hospital. Participants will be enrolled consecutively among those who provide written informed consent for collection of adenomatous and adjacent normal tissues. The study population represents adults aged 19-85 years who are clinically eligible for colonoscopy and tissue sampling",[40],{"label":41,"type":33,"description":42,"interventionNames":33},"Colorectal Adenoma Group","Participants undergoing colonoscopic polypectomy for colorectal adenoma. Adenomatous tissue and adjacent normal mucosa will be collected for methylation and sequencing analysis.",[44],{"name":45,"role":46,"phone":47,"phoneExt":33,"email":48},"OneJoong KIM, M.D.","CONTACT","82+010+2111+0415","biblian@chamc.co.kr",[50],{"facility":5,"status":33,"city":51,"state":52,"zip":53,"country":54,"countryCode":33,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Seongnam-si","Gyeonggi-do","13496","South Korea",{"type":56,"coordinates":57},"Point",[58,59],127.13778,37.43861,{"lat":59,"lon":58},[62],{"name":63,"role":46,"phone":64,"phoneExt":33,"email":48},"KIM OneJoong","01021115353",{"type":66,"investigatorFullName":63,"investigatorTitle":67,"investigatorAffiliation":5,"oldNameTitle":33,"oldOrganization":33},"PRINCIPAL_INVESTIGATOR","Clinical Assistant Professor","100621125","epigenetic-factors-of-colorectal-adenoma-in-korean-100621125",false,"NCT07366554","Epigenetic Factors of Colorectal Adenoma in Korean","Exploration of Epigenetic Factors of Colorectal Adenoma in Korean","* Inclusion Criteria:\n\n  * Adults aged 19-85 years\n  * Undergoing colonoscopic polypectomy for colorectal adenoma\n  * Able to understand the study purpose and provide written informed consent\n  * Adequate tissue available for both adenoma and adjacent normal mucosa sampling\n* Exclusion Criteria:\n\n  * History of colorectal cancer, inflammatory bowel disease, or hereditary colorectal cancer syndrome (e.g., FAP, Lynch syndrome)\n  * Previous colorectal surgery that may alter anatomy or pathology\n  * Inadequate sample quality or failure of DNA extraction\n  * Refusal or withdrawal of informed consent\n  * Severe comorbidities that make participation unsuitable at investigator's discretion","ALL","19 Years","85 Years",{"count":79,"type":80},32,"ESTIMATED","1 Day","OBSERVATIONAL","This study aims to explore epigenetic factors associated with colorectal adenoma (CRA) in the Korean population. CRA is a key precancerous lesion in the adenoma-carcinoma sequence, and identifying methylated genetic markers may improve early detection and risk stratification for colorectal cancer (CRC).\n\nA total of 32 patients undergoing colonoscopic polypectomy will be enrolled. Adenomatous and adjacent normal tissues will be collected for deoxyribonucleic acid (DNA) extraction and bisulfite conversion. Quantitative methylation-specific polymerase chain reaction (qMSP) and Sanger sequencing will be used to assess the methylation status of candidate genes (SFRP2, TFPI2, SEPT9, and SDC2). Stool samples will also be analyzed by whole-genome sequencing (WGS) to evaluate microbiome and genetic profiles.\n\nThe study seeks to determine whether methylation levels of these genes are significantly elevated in adenoma tissue compared with normal mucosa, thereby identifying potential biomarkers for colorectal neoplasia surveillance and personalized colonoscopy follow-up intervals.",[85,86],"Colorectal Adenoma","Colorectal Cancer Precancerous Lesion",[85,88,89,90,91,92,93,94,95,96,97,98],"DNA Methylation","Epigenetics","Biomarker discovery","SFRP2","TFPI2","SEPT9","SDC2","qMSP","Korean population","Colorectal cancer prevention","Adenoma-carcinoma sequence","NOT_YET_RECRUITING","2026-01-25",{"date":102,"type":103},"2026-01-27","ACTUAL",{"date":105,"type":80},"2026-02-10",{"date":107,"type":80},"2027-05-09",{"name":5,"class":6},1]