[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"manual-pressure\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:manual-pressure":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100554274","water-exchange-and-co2-insufflation-with-abdominal-compression-device-to-reduce-manual-assistance-100554274",false,"NCT06496958","Water Exchange and CO2 Insufflation With Abdominal Compression Device to Reduce Manual Assistance","CO2 Insufflation Colonoscopy With an Abdominal Compression Device and Water Exchange Colonoscopy to Reduce Manual Assistance by Endoscopy Staff: A Multicenter Randomized Trial","Inclusion Criteria:\n\n* Patients aged 45-80 years having an average risk for colorectal cancer who plan to undergo sedated outpatient colonoscopy for screening, surveillance, and those who have received a positive fecal immunochemical test result\n\nExclusion Criteria:\n\n* Patients with hereditary colorectal cancer syndrome, including familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer (Lynch syndrome)\n* Patients with serrated polyposis syndrome\n* Patients with known or suspected inflammatory bowel disease\n* Patients with a history of colorectal cancer or other intra-abdominal malignancy\n* Patients with a history of colorectal resection\n* Patients with a history of abdominal aortic aneurysm, cirrhosis, ascites, or other severe comorbid illnesses\n* Patients with recent wounds or skin rash on the anterior abdominal wall and back\n* Patients with known ventral hernia\n* Patients with unsedated procedure\n* Patients with planned bidirectional endoscopy\n* Patients with body mass index \\>35 kg\u002Fm2\n* Patients with waist circumference \\\u003C55 cm or \\>105 cm\n* Patients with known or suspected gastroparesis\n* Patients with planned therapeutic procedures (e.g., hemostasis, removal of a large polyp)\n* Patients with mental retardation\n* Pregnant women or those planning pregnancy\n* Patients unwilling to participate in the study",true,"ALL","45 Years","80 Years",{"count":21,"type":22},400,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this trial is to evaluate whether water exchange colonoscopy and CO2-insufflation colonoscopy with an abdominal compression device (Maxbelt me3 type, Nippon Sigmax Co., Tokyo, Japan) can achieve a significantly lower proportion of patients requiring manual abdominal pressure during colonoscopic insertion compared with CO2 insufflation alone.",[28,29,30,31],"Manual Pressure","Repositioning","Colonoscopy","Colon Polyp","RECRUITING","2024-11-03",{"date":35,"type":36},"2024-11-05","ACTUAL",{"date":38,"type":36},"2024-09-02",{"date":40,"type":22},"2026-09-30",{"name":42,"class":43},"Evergreen General Hospital, Taiwan","OTHER",2]