[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"bowel-sounds\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:bowel-sounds":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":4},"100649924","detection-of-infant-gastrointestinal-activity-using-sound-technology-100649924",false,"NCT07743216","Detection of Infant GastrointEstinal Activity Using Sound Technology","DIGEST","Inclusion Criteria:\n\n* ≥ 37 weeks Gestational Age (GA)\n\nExclusion Criteria:\n\n* Congenital anomalies\n* Gastrointestinal abnormalities or disorders\n* Low birth weight (\\\u003C 2500 g)\n* Maternal magnesium sulfate exposure prior to delivery\\*\n* Fragile skin or skin conditions precluding sensor placement","ALL","1 Minute","30 Weeks",{"count":20,"type":21},10,"ESTIMATED","OBSERVATIONAL","This pilot study aims to evaluate the feasibility and safety of continuous bowel sound monitoring in healthy term newborn infants using a novel wireless acoustic monitoring system. Participants will undergo a single 4-hour recording during routine postnatal care while bowel sounds are continuously recorded using wearable abdominal sensors. Feasibility will be assessed by participant recruitment and study completion, as well as the acquisition of high-quality, analyzable acoustic data. Bowel sounds will be characterized by assessing the temporal and spectral features of bowel sounds during the early neonatal period and exploring their relationship with routine caregiving activities and feeding.",[25,26,27,28],"Infant, Newborn, Diseases","Bowel Sounds","Physiologic Monitoring","Wearable Sensors","NOT_YET_RECRUITING","2026-07-29",{"date":32,"type":33},"2026-08-03","ACTUAL",{"date":35,"type":21},"2026-09-01",{"date":37,"type":21},"2027-12-01",{"name":39,"class":40},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":53,"studyType":22,"phases":4,"briefSummary":54,"conditions":55,"keywords":60,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100647184","the-value-of-bowel-sounds-in-evaluating-postoperative-intestinal-function-recovery-in-colorectal-cancer-patients-100647184","NCT07705139","The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal Cancer Patients","The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal Cancer Patients: A Prospective Cohort Study","BRIEF","Inclusion Criteria:\n\n* Aged 18-80 years.\n* Histopathologically confirmed colorectal adenocarcinoma according to the WHO 2022 classification.\n* No restriction on prior neoadjuvant or other antitumor therapies, including chemotherapy, radiotherapy, targeted therapy, or immunotherapy.\n* Able to understand the study requirements and voluntarily provide written informed consent (patient and\u002For legally authorized representative).\n* Able to communicate effectively with the investigators and willing to comply with all study procedures, including postoperative management and follow-up.\n\nExclusion Criteria:\n\n* Significant organ dysfunction indicating inability to tolerate surgery or an unacceptably high perioperative risk, including:\n* Severe cardiac dysfunction (NYHA Class III or IV).\n* Severe hepatic dysfunction (MELD score \\>12).\n* Severe renal dysfunction (eGFR \\\u003C30 mL\u002Fmin\u002F1.73 m² \\[CKD stage 4-5\\] or end-stage renal disease requiring dialysis).\n* Severe pulmonary dysfunction (resting PaO₂ \\\u003C60 mmHg on room air or respiratory failure requiring long-term oxygen therapy or mechanical ventilation).\n* Participation in another clinical study within 4 weeks before enrollment or concurrent participation in another interventional clinical study.\n* Emergency surgery required because of intestinal obstruction, perforation, or other acute abdominal conditions.\n* Severe psychiatric disorders that would interfere with compliance with perioperative management or follow-up.\n* Pregnant or breastfeeding women.\n* Any other clinical or laboratory abnormality that, in the opinion of the investigator, would make the participant unsuitable for the study.","18 Years","90 Years",{"count":52,"type":21},172,"30 Days","This study enrolls patients scheduled to undergo curative surgery for colorectal cancer. Bowel sounds will be assessed preoperatively and postoperatively. By comparing intraoperative variables, the incidence of perioperative complications, reoperation rates, and postoperative outcomes-including time to first flatus, resumption of oral intake, and occurrence of intestinal obstruction-this study aims to investigate the association between perioperative bowel sounds and postoperative recovery, and provide evidence-based support for the clinical application of bowel sound monitoring.\n\nSupplementary Definitions",[26,56,57,58,59],"Colorectal Cancer","Intestinal Obstruction","Postoperative Ileus","Colorectal Surgery",[61,56,57,58,59],"bowel sounds","RECRUITING","2026-07-09",{"date":65,"type":33},"2026-07-15",{"date":67,"type":33},"2026-02-01",{"date":69,"type":21},"2026-07-28",{"name":71,"class":40},"Zhongnan Hospital",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":83,"phases":84,"briefSummary":86,"conditions":87,"keywords":91,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":72},"100481061","spectral-analysis-of-bowel-sounds-in-preterm-babies-of-less-than-32-weeks-of-amenorrhea-wa-as-predictive-factor-of-enterocolitis-100481061","NCT05544097","Spectral Analysis of Bowel Sounds in Preterm Babies of Less Than 32 Weeks of Amenorrhea (WA) as Predictive Factor of Enterocolitis","BHAPE","Inclusion Criteria:\n\n* preterm babies of less than 32WA\n\nExclusion Criteria:\n\n* preterm babies of more than 32WA,\n* digestive congenital malformation","32 Weeks",{"count":82,"type":21},50,"INTERVENTIONAL",[85],"NA","The recording or bowels is easy and cheap. The investigators wonder if these sounds are modified in babies with high risk of necrotizing enterocolitis. In this study, the investigators suggest to record and do a spectral analysis of 30 seconds of bowel sounds in preterm babies of less than 32WA before and after enteral nutrition, every day until the end of hospitalization. A spectral analysis will be made for each record to determine frequencies of the signal. The investigators will try to determine physiological frequencies and look for modifications in pathological situations.",[26,88,89,90],"Spectral Analysis","Necrotizing Enterocolitis","Preterm Babies",[61,92,89,93],"spectral analysis","preterm babies","2024-07-09",{"date":96,"type":33},"2024-07-10",{"date":98,"type":33},"2022-09-06",{"date":100,"type":21},"2025-11",{"name":102,"class":40},"Centre Hospitalier Universitaire, Amiens"]