[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"colorectal-sessile-serrated-lesion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:colorectal-sessile-serrated-lesion":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100650303","impact-of-linked-color-imaging-on-sessile-serrated-lesion-miss-rate-100650303",false,"NCT07745842","Impact of Linked Color Imaging on Sessile Serrated Lesion Miss Rate","Impact of Linked Color Imaging on Sessile Serrated Lesion Miss Rate: a Multicenter Tandem Rondomized Controlled Trial","Inclusion Criteria:\n\n1. Subjects aged ≥45 years, regardless of gender;\n2. Subjects undergoing screening colonoscopy;\n3. Subjects with no prior colonoscopy;\n4. Voluntarily provide written informed consent.\n\nExclusion Criteria:\n\n1. Subjects unable to cooperate with or tolerate colonoscopy;\n2. Subjects with inflammatory bowel disease;\n3. Known or highly suspected colorectal obstruction;\n4. History of colorectal surgery;\n5. Chronic recurrent constipation;\n6. Failure to discontinue anticoagulants or antiplatelet agents for at least 1 week before the procedure;\n7. Poor bowel preparation with an inadequate Aronchick scale score during colonoscopy;\n8. Failed cecal intubation;\n9. High-risk conditions including severe cardiovascular and cerebrovascular diseases, uncorrected severe anemia or active infection;\n10. Pregnant or breastfeeding women;\n11. Subjects deemed ineligible for participation in this trial at the investigator's discretion.",true,"ALL","45 Years",{"count":20,"type":21},2072,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective, multicenter randomized controlled trial aimed to investigate whether linked color imaging (LCI) could reduce the miss rate of sessile serrated lesions (SSLs) during tandem colonoscopy compared with conventional white-light imaging (WLI).",[27],"Colorectal Sessile Serrated Lesion","NOT_YET_RECRUITING","2026-07-30",{"date":31,"type":32},"2026-08-04","ACTUAL",{"date":34,"type":21},"2026-08",{"date":36,"type":21},"2029-02",{"name":38,"class":39},"Nanfang Hospital, Southern Medical University","OTHER",{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":17,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":22,"phases":51,"briefSummary":52,"conditions":53,"keywords":54,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":67},"100562889","emr-versus-csp-in-the-treatment-of-sessile-serrated-lesions-less-than-10mm-in-size-100562889","NCT06609031","EMR Versus CSP in the Treatment of Sessile Serrated Lesions Less Than 10mm in Size","Endoscopic Mucosal Resection Versus Cold Snare Polypectomy in the Treatment of Sessile Serrated Lesions Less Than 10mm in Size: a Single-center, Open-label, Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged between 35 and 75 years\n* Suspected sessile serrated lesions less than 10mm in size in screening, surveillance or therapeutic colonoscopy\n* 0-Is or 0-IIa according to Paris classification\n* Type 1 according to NICE and JNET classification\n* Type II according to pit pattern\n* Patients must sign an informed consent form prior to registration in study\n\nExclusion Criteria:\n\n* Unsuitable for removal by EMR or CSP\n* Suspected dysplasia or malignancy\n* Recurrent sessile serrated lesions after endoscopic resection\n* Familial adenomatous polyposis, Lynch syndrome or serrated polyposis syndrome\n* History of inflammatory bowel disease\n* Patients taking anticoagulant and antiplatelet agents before the examination\n* Severe illness or other high-risk conditions that prevent the patient from cooperating with or tolerating endoscopic therapy\n* Refusal to sign the informed consent form or any other factors that are not suitable for enrollment or affect the ability to participate in the study","35 Years","75 Years",{"count":50,"type":21},270,[24],"A prospective, single-center, open-label, randomized controlled study to compare the effectiveness and safety of endoscopic mucosal resection (EMR) and cold snare polypectomy (CSP) in treating colorectal sessile serrated lesions (SSLs) less than 10mm in size.",[27],[55,56,57],"Sessile Serrated Lesion","cold snare polypectomy","endoscopic mucosal resection","2024-09-23",{"date":60,"type":32},"2024-09-25",{"date":62,"type":21},"2024-10-01",{"date":64,"type":21},"2026-10-01",{"name":66,"class":39},"Fudan University",1]