[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"gastrostomy-complications\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:gastrostomy-complications":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,72],{"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":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100513503","pediatric-percutaneous-ultrasound-gastrostomy-technique-100513503",false,"NCT05966311","Pediatric Percutaneous Ultrasound Gastrostomy Technique","A Multi-center, Feasibility Study to Evaluate the Use and Safety and of the Pediatric PUMA-G System for Percutaneous Ultrasound Gastrostomy","Inclusion Criteria:\n\n* Informed consent must be obtained from the patient or a Legally Authorized Representative (ex. parent\u002Fguardian) before any study-specific assessment is performed\n* Weight ≥5 (Phase 0, Phase 1, Phase 2)\n* Weight ≥3kg and \\\u003C10kg (Phase 3)\n* Estimated abdominal wall thickness ≤3cm\n* Indication for gastrostomy tube placement, with or without jejunal access tubing via gastrostomy tract, determined to be present for any of the following reasons:\n* Anatomic: Ear, nose, or throat abnormalities (Pierre-Robin sequence cleft lip palate)\n* Neurologic: Head trauma, Cerebral palsy\n* Bowel Disease: Short Bowel syndrome, intestinal dysmotility, inflammatory bowel disease, malabsorption\n* Failure to Thrive: Cystic Fibrosis, Cholestasis, AID, Chronic renal failure, and food refusal\n* Patient determined to be an appropriate candidate for PUG, PEG, or PRG by the clinical care team\n* Anticipated discharge \\> 24 hrs following gastrostomy\n\nExclusion Criteria:\n\n* Temperature ≥ 38 C\n* Systolic BP \\\u003C 80 or \\> 180 mmHg\n* Heart Rate \\\u003C 50 or \\> 160\n* Estimated abdominal wall thickness \\>3cm\n* Coagulopathy defined by INR \\> 1.7 or Platelets \\\u003C50,000\n* Presence of a contraindication to being in proximity to a magnet (e.g. implantable metallic device).\n* History of prior gastrostomy, gastrectomy (partial or complete), or abdominal trauma or upper-abdominal surgery.\n* Scoliosis\n* Atypical organ placement including microgastria\n* Involvement in other investigational trials within 30 days prior to screening,\n* Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test\n* Patients with HgB \\\u003C 7g\u002FdL, or fluid resuscitated within 48hrs prior, or received blood transfusion within 48hrs prior, or active life threatening GI bleeding\n* Esophageal Diseases: Atresia, stricture, caustic ingestion\n* Spinal anomalies or atypical organ placement\n* Any other medical condition(s) that may put the patient at risk or influence study results in the investigator's opinion, based on the performance of a pre-procedural assessment.","ALL","0 Years","21 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this research study is to test a new device called the PUMA-G Pediatric System. The research will measure if the device works well to safely aid doctors placing gastrostomy feeding tubes in children. The PUMA-G Pediatric System is an investigational device that uses ultrasound and magnets to guide insertion of a feeding tube.",[27,28,29,30],"Gastrostomy","Gastrostomy Complications","Pediatric Disorder","Ultrasound",[27,32,33,34,30,35],"Pediatric Gastrostomy","Device Feasibility","Device Safety","POCUS","RECRUITING","2026-07-30",{"date":39,"type":40},"2026-07-31","ACTUAL",{"date":42,"type":40},"2023-07-07",{"date":44,"type":21},"2028-12-31",{"name":46,"class":47},"CoapTech","INDUSTRY",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":71},"100486770","pain-assessment-following-placement-of-a-percutaneous-radiologic-gastrostomy-and-predictive-factors-100486770","NCT05618392","Pain Assessment Following Placement of a Percutaneous Radiologic Gastrostomy and Predictive Factors","DOULEURGPR","Inclusion Criteria:\n\n* Needing a radiologic gastrostomy under local anesthesia\n* Age ≥ 18 years old\n* Read, write and understand the French language\n\nExclusion Criteria:\n\n* Patient under guardianship, deprived of liberty, safeguard of justice\n* Patient presenting a serious psychiatric pathology that does not allow compliance with the completion of the questionnaires (at the discretion of the investigator)\n* Refusal to participate in research","18 Years",{"count":57,"type":21},50,"OBSERVATIONAL","A 12 months mono-center, descriptive study, to evaluate pain and predictive factors Following placement of percutaneous Radiologic gastrostomy (PRG).\n\nThe primary objective is to evaluate the abdominal pain associated with percutaneous radiologic gastrostomy (PRG) placement.",[28,27],"2026-03-17",{"date":63,"type":40},"2026-03-18",{"date":65,"type":40},"2022-12-09",{"date":67,"type":21},"2026-09-01",{"name":69,"class":70},"Centre Hospitalier de Valence","OTHER",1,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":87,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":71},"100616073","does-the-thickness-of-the-gastrostomy-affect-the-incidence-of-complications-a-prospective-randomized-single-center-study-in-children-100616073","NCT07300865","Does the Thickness of the Gastrostomy Affect the Incidence of Complications? A Prospective Randomized Single-Center Study in Children","Inclusion Criteria:\n\n* Scheduled for laparoscopic gastrostomy at Dep Pediatric Surgery Uppsala Akademiska University Hospital\n\nExclusion Criteria:\n\n* Any specific reasons to avoid one size or the other (children who are supposed to get mixed food or a special medication that can obstruate the tube will recieve a thicker tube)","15 Years",{"count":80,"type":21},200,[24],"The goal of this interventional study is to compare two different sizes of a gastrostomy tube in children and the incidence of complications three months postoperatively. The study is questionnare-based and both the family and health care personel will fill in the formula about complications at the re-visit when the tube is changed the first time at three months postoperatively. Complications requested are: granuloma, infection, pain, dislocation and leakage.",[28,84,85,86],"Gastrostomy Size","Food Intolerance","Granuloma",[88,89,90,91,92],"laparoscopic gastrostomy","complications","pediatric surgery","children","granuloma","2025-12-20",{"date":95,"type":40},"2025-12-24",{"date":97,"type":40},"2025-11-20",{"date":99,"type":21},"2030-01-01",{"name":101,"class":70},"Therese Hössjer"]