[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"enteral-feeds\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:enteral-feeds":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100625461","plant-protein-dominant-tube-feed-study-100625461",false,"NCT07422935","Plant-Protein Dominant Tube Feed Study","Exploratory Randomised, Controlled Trial To Evaluate The Impact Of Four Nutritionally Complete, Plant-Protein Dominant, Enteral Tube Feeds On Long Term Outcomes In Community-Based Adults","Inclusion Criteria:\n\n* Male or female\n\n  -≥16 years of age\n* Using or requiring an enteral tube feed in the community as part of nutritional management plan\n* Expected to receive at least 500ml (≥500kcal) per day from one of the study products\n\nExclusion Criteria:\n\n* Receiving parenteral nutrition\n* Patients with major hepatic dysfunction (i.e., decompensated liver disease)\n* Patients with major renal dysfunction (i.e., requiring filtration or stage 4\u002F5 chronic kidney disease (CKD))\n* Patients receiving inpatient care\n* Known pregnancy or lactation\n* Participation in other clinical intervention studies within 1 month of this study\n* Allergy to any study product ingredients\n* Investigator concern regarding ability or willingness of patient to comply with the study requirements.","ALL","16 Years",{"count":19,"type":20},110,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study aims to determine whether a reformulated plant-protein dominant protein blend in four existing enteral tube feeds is as effective as animal-protein dominant formulations in patients who are tube fed at home. This is an exploratory randomised, controlled, trial with a 3-day baseline period. Adult home tube feeding patients will be randomised to receive either a plant-protein dominant formulation or a control product (an animal-protein dominant formulation) for a 3-month intervention period followed by a 6-month and 12-month follow-up. The outcomes include gastrointestinal tolerance, compliance, acceptability, anthropometry, nutrient intake, and physical function",[26,27],"Enteral Nutrition (Food for Special Medical Purposes)","Enteral Feeds","RECRUITING","2026-02-13",{"date":31,"type":32},"2026-02-20","ACTUAL",{"date":34,"type":32},"2026-01-01",{"date":36,"type":20},"2027-03",{"name":38,"class":39},"Nutricia UK Ltd","INDUSTRY",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":48,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":57,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":40},"100567046","using-nirs-to-evaluate-splanchnic-oxygenation-during-blood-transfusion-in-preterm-infant-100567046","NCT06663085","Using NIRS to Evaluate Splanchnic Oxygenation During Blood Transfusion in Preterm Infant","The Effect of Enteral Feeding on Splanchnic Oxygenation During Blood Transfusion in Preterm Infants","Inclusion Criteria:\n\n* Infant with gestational age \\\u003C 37 weeks\n* Planned to receive blood transfusion\n* Had received minimum 25 ml\u002Fkg\u002Fday enteral feeding\n* in stable condition\n\nExclusion Criteria:\n\n* Infant with multiple congenital anomalies\n* Infant with suspected\u002Fconfirmed genetic anomalies\n* Parents or family did not sign the informed consent",true,{"count":50,"type":20},42,[23],"To evaluate the differences splanchnic oxygen saturation in preterm infants receiving red blood cell transfusion with and without enteral feeding, and their outcomes.",[54,55,56,27],"Splanchnic Oxygenation","NIRS","PreTerm Neonate",[58,59,60,61,62],"transfusion","nirs","splanchnic oxygenation","preterm neonate","enteral feeds","NOT_YET_RECRUITING","2024-10-28",{"date":66,"type":32},"2024-10-29",{"date":68,"type":20},"2024-10-30",{"date":70,"type":20},"2025-01-15",{"name":72,"class":73},"Gadjah Mada University","OTHER"]