[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ileostomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ileostomy":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,74],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100614773","diverting-ileostomy-and-transverse-colostomy-comparative-study-100614773",false,"NCT07283952","Diverting Ileostomy and Transverse Colostomy Comparative Study","Diverting Ileostomy Verses Transverse Colostomy in Colorectal Surgery","Inclusion Criteria:\n\n* • Adults ≥18 years undergoing elective low anterior resection or coloanal anastomosis for benign or malignant colorectal disease.\n\n  * Patients for whom the surgeon has decided that a diverting stoma is required such as emergency resection and anastomosis cases where a covering stoma is indicated.\n  * Ability to provide informed consent.\n\nExclusion Criteria:\n\n* • Patients with pre-existing stoma.\n\n  * Severe comorbidities precluding stoma creation (e.g., advanced renal failure, uncontrolled cardiac disease).\n  * Patients with extensive peritoneal carcinomatosis or unresectable disease.\n  * Pregnant or lactating women.\n  * Inability to comply with follow-up or provide informed consent.","ALL","18 Years","80 Years",{"count":20,"type":21},36,"ESTIMATED","INTERVENTIONAL",[24],"NA","Protective diverting stomas are frequently constructed after low anterior resection or colorectal anastomosis to mitigate the consequences of anastomotic leakage, one of the most feared complications in colorectal surgery.\n\nBoth loop ileostomy (LI) and loop transverse colostomy (TC) are accepted methods of diversion. Randomized and observational studies have shown that faecal diversion significantly reduces the clinical severity of leaks and the need for reoperation compared with no diversion.\n\nThe choice between LI and TC remains controversial. Loop ileostomy is technically straightforward and associated with shorter operative time and fewer septic complications at closure. However, it carries specific risks, including high-output stoma, dehydration, electrolyte imbalance, and renal impairment, which may lead to hospital readmissions. Conversely, loop transverse colostomy is associated with fewer fluid and electrolyte issues, but has higher rates of prolapse, skin irritation, and wound complications at closure.\n\nMeta-analyses comparing LI and TC indicate no clear superiority, with each approach demonstrating distinct patterns of morbidity. Some randomized trials have suggested lower major morbidity with LI, while others found no significant difference. Given the heterogeneity of outcomes and limited high-quality, adequately powered trials, further randomized evidence is needed to guide optimal stoma selection in colorectal surgery.",[27,28,29],"Ileostomy","Colostomy","Colorectal Surgery",[31,32,29],"Diverting Ileostomy","Transverse Colostomy","NOT_YET_RECRUITING","2025-12-12",{"date":36,"type":37},"2025-12-16","ACTUAL",{"date":39,"type":21},"2026-01-30",{"date":41,"type":21},"2027-11-30",{"name":43,"class":44},"Assiut University","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":4},"100612973","effect-of-a-mobile-application-on-stoma-adaptation-and-quality-of-life-100612973","NCT07260539","Effect of a Mobile Application on Stoma Adaptation and Quality of Life","The Effect of Education, Counseling, and Monitoring Provided to Individuals With Stoma Via a Mobile Application on Adaptation to Stoma and Quality of Lif","STOMATERAPİ-M","Inclusion Criteria:\n\nAge ≥18 years Able to read and write Turkish Undergoing ostomy surgery for the first time Permanent ostomy or expected to remain for at least 6 months No major mental, physical, or communication impairment Owns an iOS\u002FAndroid smartphone with active internet access Able to use mobile applications Uses WhatsApp for digital form submission during follow-up\n\nExclusion Criteria:\n\nReceiving stoma-related education or counseling from another institution or professional during the study period",{"count":54,"type":21},66,[24],"This single-blind, parallel-group randomized controlled trial aims to evaluate the effects of a mobile app-based education, counseling, and follow-up program on stoma adaptation and quality of life in adults with a newly ostomy. The study will be conducted at the Stomatherapy Unit of Gazi University Health Research and Application Center (Ankara, Turkey). Participants meeting the inclusion criteria (n=66) will be assigned to intervention (mobile app support + standard care) and control (standard care only) groups in a 1:1 ratio via block randomization; participants will be kept unaware of their group assignment. Participants in the intervention group will download the \"Stomatherapy-M\" app on the day of discharge and will access structured educational content, receive nurse counseling (messaging and scheduled video calls), and share scheduled follow-up records regularly for six months. Follow-up frequency will be weekly in the first month, biweekly in the second month, and monthly in the following months. Primary outcomes; Adaptation to the stoma (Ostomy Adjustment Inventory) and stoma-related quality of life (Quality of Life Adaptation Scale) assessed at 15 days and 1, 3, and 6 months after discharge. App usability (MAUS) will be measured at 6 months only in the intervention group.",[58,27,59],"Intestinal Stoma","Colostomy - Stoma",[61,62,63,64],"Mobile application","ostomy","adaptation","quality of life","2025-11-21",{"date":67,"type":37},"2025-12-03",{"date":69,"type":21},"2026-01-01",{"date":71,"type":21},"2026-12-30",{"name":73,"class":44},"Gazi University",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":87,"overallStatus":92,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100562506","a-study-comparing-laparoscopicrobotic-stoma-reduced-port-fusion-surgery-with-traditional-surgery-in-patients-with-temporary-ileostomy-100562506","NCT06604052","A Study Comparing Laparoscopic\u002FRobotic Stoma Reduced-Port Fusion Surgery with Traditional Surgery in Patients with Temporary Ileostomy","A Prospective, Randomized, Parallel-Controlled Study Comparing Laparoscopic\u002FRobotic Stoma Reduced-Port Fusion Surgery with Traditional Surgery in Patients with Temporary Ileostomy","FUSION","Inclusion Criteria:\n\n1. After preoperative evaluation, patients scheduled for laparoscopic\u002Frobotic colorectal surgery (rectum, sigmoid colon, left colon) who are planned to undergo prophylactic ileostomy.\n2. No serious systemic infection or immunosuppression.\n3. Over 18 years of age.\n4. Eastern Cooperative Oncology Group Performance Status: 0-1\n5. The expected survival time \\> 6 months.\n6. The subjects voluntarily participate and sign the informed consent\n\nExclusion Criteria:\n\n1. Any skin infectious diseases in the abdominal wall.\n2. Use hormones and immunosuppressive drugs within 1 month before surgery.\n3. The time between operation and the last chemotherapy was less than 1 month.\n4. Any previous ostomy surgery.\n5. Any serious active infection or uncontrollable infection that requires systematic treatment.\n6. A clear history of neurological or psychiatric disorders.\n7. Subjects may not be able to complete the study for other reasons.",{"count":83,"type":21},80,[24],"The traditional positioning and surgical methods for temporary ileostomy no longer meet the requirements of minimally invasive surgery: (1) Conventional stoma positioning often leads to the trocar incision being too close to the stoma site, increasing the risk of baseplate leakage and skin infection. (2) Since stoma positioning is required to be within the rectus abdominis, the proximity between the stoma and auxiliary incision can heighten difficulties in stoma bag attachment and raises the risk of fecal leakage. (3) Stoma retraction surgery within the rectus abdominis is more traumatic and complex. We introduce for the first time a modified stoma positioning and surgical method, termed Reduced-Port Fusion Surgery. This technique includes preoperative trocar\u002Fstoma fusion positioning and intraoperative trocar\u002Fstoma fusion surgery. The procedure is based on the 3R principles: Reposition - the stoma is repositioned within the Joint Trocar\u002FStoma Zone, allowing for more lateral placement to meet surgical needs without being confined to the rectus abdominis. Reduce Port - the same fusion point is used for both trocar insertion and stoma creation, enabling dual use of one site. Recognize - surgeons participate in stoma positioning, recognize the positioning, and follow the procedure. This prospective, randomized, parallel-controlled clinical study aims to evaluate whether Reduced-Port Fusion Surgery can reduce stoma-related complications, postoperative pain, improve quality of life, and facilitate stoma retraction surgery compared to traditional methods. A total of 80 participants will be randomly assigned in a 1:1 ratio. The experimental group will undergo Reduced-Port Fusion Surgery while the control group will receive traditional surgery.",[27],[88,89,90,91],"ileostomy","minimally invasive surgery","Reduced-Port Fusion Surgery","stoma complication","RECRUITING","2024-09-17",{"date":95,"type":37},"2024-09-19",{"date":97,"type":37},"2024-09-06",{"date":99,"type":21},"2025-12-31",{"name":101,"class":44},"Xinhua Hospital, Shanghai Jiao Tong University School of Medicine",1]