[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tube-feeding\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tube-feeding":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100636811","tubeclear-system-evaluation-in-pediatric-patients-100636811",false,"NCT07570537","TubeClear System Evaluation in Pediatric Patients","Inclusion Criteria:\n\n* Males or females under the age of 18 for the entire duration of the study procedure and follow up with an occluded (partial\u002Fsluggish or fully blocked) EAD\n* Indwelling EAD must be NE, NG, NJ tube composed of PVC or polyurethane and is 6-18 FR, 38-140 cm\n* NG tube being used as a J tube inserted through a G tube and is 6-18 Fr; 38-140 cm\n* G and J tubes 10-18 Fr; 20-36cm\n* Specific GJ tubes: G-Jet, MIC, and MIC-KEY Tubes that are size 14-22Fr and have a jejunal length of 15-45cm\n\nExclusion Criteria:\n\n* Wards of the State\n* Positive urine pregnancy test\u002Fpregnant females or inability to take a pregnancy test\n* Any active gastrointestinal abnormalities, including but not limited to infections, inflammation, and\u002For recent abdominal surgery (except for recent gastrostomy placement) or trauma\n* Constant dependency on the EAD for glucose source\n* Unable to tolerate water volume needed for EAD flush\n* Unknown length of EAD\n* Attending physician declines enrollment based on clinical judgment\n* Subject turns 18 years of age during study duration\n* Very low birth weight (\\\u003C1.5kg)","ALL","0 Years","17 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","Enteral access devices (EADs) provide necessary hydration, nutrition, and medications to numerous patients in hospitals across the United States. When patient's EAD becomes clogged it can delay administration of important nutrition and medications which can cause adverse effects such as malnutrition, and dehydration, especially in pediatric patients. Traditional methods of unclogging EADs can require the use of special enzymes or chemicals but these produce a variable rate of success. The TubeClear system has been developed to help alleviate the need for use of special enzymes or chemicals and to provide a quick, safe alternative for those with a clogged or sluggish EAD all while at the patient's bedside. This system prevents the need for subsequent exposure to radiation and contrast media for confirmation of EAD location after replacement.",[26,27,28,29,30,31],"Clogged Enteral Access Devices","Occluded Enteral Access Devices","Enteral Nutrition","Enteral Access Device","Tube Feeding","Gastric Feeding Tubes","NOT_YET_RECRUITING","2026-06-04",{"date":35,"type":36},"2026-06-05","ACTUAL",{"date":38,"type":20},"2026-07-01",{"date":40,"type":20},"2028-06-01",{"name":42,"class":43},"Children's Mercy Hospital Kansas City","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":15,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100601795","efficacy-of-a-novel-prototype-gastrostomy-tube-anchor-dressing-100601795","NCT07115134","Efficacy of a Novel Prototype Gastrostomy Tube Anchor Dressing","Tube Anchor","Inclusion Criteria:\n\n* Patients who are undergoing gastrostomy tube placement or are within five days post-operatively of gastrostomy tube placement.\n\nExclusion Criteria:\n\n* 1\\. Patients with a skin condition that limits the placement of the dressing, this will be confirmed with the clinical team","7 Years","21 Years",{"count":54,"type":20},75,[23],"This is a single-center prospective study evaluating the efficacy of a prototype gastrostomy anchor dressing for use with button gastrostomy tubes. The anchor dressing has been previously evaluated for usability by parents, patients, and nurses. This study compares several outcomes related to complications from gastrostomy tube placement using a prospective cohort of patients and a retrospective analysis of complications associated with gastrostomy tubes. Prospective patients will initially be monitored until they have completed their last dressing change or for a maximum of 50 days. They will then complete their final survey. Their charts will be reviewed for up to one year from their initial gastrostomy placement. The study's primary objective is to determine if the novel gastrostomy tube anchor dressing reduces rates of gastrostomy tube dislodgement and ED\u002Fclinic visits for gastrostomy tube complications.",[58,30],"Gastroenterology Surgery","RECRUITING","2025-08-04",{"date":62,"type":36},"2025-08-11",{"date":64,"type":36},"2024-09-24",{"date":66,"type":20},"2027-12-18",{"name":68,"class":43},"Children's National Research Institute",1]