[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"paediatric\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:paediatric":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,44,68,101,126,155],{"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":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100645352","relational-music-therapy-procedural-support-for-paediatric-patients-and-families-facing-repeated-invasive-procedures-100645352",false,"NCT07680348","Relational Music Therapy Procedural Support for Paediatric Patients and Families Facing Repeated Invasive Procedures","Relational Regulation: A Relational Approach to Music Therapy-based Procedural Support for Paediatric Patients and Families Facing Repeated Invasive Procedures","Inclusion Criteria:\n\n* Paediatric patient (ages 5-12) undergoing recurring needle procedures (venipuncture, intravenous (IV) cannulation, subcutaneous injections, intramuscular (IM) injections, Port-a-Cath, lumbar punctures, and bone marrow transplant, aspiration or biopsy)\n* Parents or caregiver of a paediatric patient (ages 5-12) undergoing recurring needle procedures.\n* Willing to participate in music therapy-based sessions.\n* Able to complete brief questionnaires and\u002For take part in an interview.\n* Paediatric inpatient, outpatient, or palliative care unit.\n\nExclusion Criteria:\n\n* Patients currently under heavy sedation or anaesthetic medication that impairs consciousness during data collection.\n* Medically unstable or emergency care patients where participation may interfere with clinical care.\n* Non-English or non-Norwegian speakers where language barriers may pose difficulties in participants understanding study information, and issues in interpretation and analysis of collected data.\n* Patients with severe cognitive or developmental impairment making meaningful engagement with the intervention difficult.\n* Severe behavioural\u002Fpsychiatric conditions that will make safe participation difficult or impossible.","ALL","5 Years","12 Years",{"count":20,"type":21},20,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study explores how personalised music therapy can support children and their parents during repeated medical procedures, such as blood tests or injections. Many children find these procedures painful or frightening, and repeated experiences can lead to high anxiety and difficulty coping. Parents often feel distressed as well, which can affect how well they are able to support their child. Because children and parents regulate each other emotionally, helping both members of the pair is important for reducing distress.\n\nThis study aims to explore how personalised music therapy-based procedural support (MTPS) influences the relational and emotional processes that help children and their parents cope, regulate, and build resilience during repeated medical procedures.",[27,28,29,30,31],"Paediatric","Invasive Procedure","Relation, Family","Music Therapy","Procedural Fear","NOT_YET_RECRUITING","2026-06-25",{"date":35,"type":36},"2026-07-02","ACTUAL",{"date":38,"type":21},"2026-09",{"date":40,"type":21},"2027-01",{"name":42,"class":43},"Anglia Ruskin University","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":4},"100643554","effects-of-a-therapeutic-strength-training-programme-in-paediatric-cancer-patients-100643554","NCT07638163","EFFECTS OF A THERAPEUTIC STRENGTH TRAINING PROGRAMME IN PAEDIATRIC CANCER PATIENTS","EFFECTS OF A THERAPEUTIC STRENGTH TRAINING PROGRAMME ON QUALITY OF LIFE, FUNCTIONAL ABILITY AND MENTAL HEALTH IN PAEDIATRIC CANCER PATIENTS","Inclusion Criteria:\n\n* People under the age of 18 who have been diagnosed with cancer and are currently undergoing treatment or living with the after-effects of the disease.\n* People who have not engaged in regular physical activity in the last 8 weeks.\n* Performance Status (ECOG) 0-1.\n* Signing of the informed consent form.\n\nExclusion Criteria:\n\n* Have any contraindications to physical exercise: severe musculoskeletal disorders, severe cardiovascular diseases, uncontrolled bone metastases, and other conditions as determined by a healthcare professional.\n* Patients who are unable to undergo the initial assessment tests or who have difficulty performing basic exercises.\n* Patients who must discontinue treatment due to intolerance to it.\n* Other circumstances, at the discretion of the investigators, that may interfere with the purpose or conduct of the study.","18 Years",{"count":20,"type":21},[24],"This project is made possible through the Pediatrics Department of the University Hospital of Salamanca, in collaboration with researchers specialized in therapeutic exercise from other clinical trials and research projects, alongside physical therapists experienced in designing, programming, and supervising therapeutic exercise programs.\n\nFurthermore, the project addresses current healthcare needs, as a significant portion of the patient population exhibits symptoms that impair functional capacity and overall quality of life-driven both by age and the oncological disease and its treatment. Consequently, this initiative aims to implement a strength training program to foster beneficial outcomes across various aspects of these patients' health, while sharing the findings with the scientific community.",[56,27],"Cancer",[56,58,27],"Exercise","2026-06-04",{"date":61,"type":36},"2026-06-10",{"date":63,"type":21},"2026-05-30",{"date":65,"type":21},"2026-12-30",{"name":67,"class":43},"University of Salamanca",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":16,"minAge":75,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":100},"100608702","beluga-better-to-exchange-ett-for-lma-before-extubation-in-children-under-general-anaesthesia-100608702","NCT07204990","BELUGA: Better to Exchange ETT for LMA Before Extubation in Children Under General Anaesthesia","BELUGA","Participant Inclusion Criteria\n\n* Children 0-16 years,\n* 5kg and above,\n* presenting for elective, semi-elective or emergency surgery under general anaesthesia\n* With airway management planned with an endotracheal tube.\n\nExclusion Criteria:\n\n* Children with severe cardiopulmonary disease or syndrome\n* Children \\\u003C 5kg\n* Children with a contraindication to deep removal of ETT deep or exchange of ETT to LMA at the end of the case (e.g. high risk of aspiration)\n* Children with a known or anticipated difficult airway\n* Children remaining intubated post-procedure\n* Children undergoing major airway surgery or bronchoscopies","0 Years","16 Years",{"count":78,"type":21},1400,[24],"During surgery, anaesthetists can use an endotracheal tube (ETT) to facilitate ventilation. At emergence from general anaesthesia, there are two techniques for removal of the ETT: (1) the ETT is removed when the child is waking up in (awake removal); or (2) the ETT is removed while still under anaesthesia(deep removal).\n\nCurrently there is no evidence to suggest either technique is safer - deep removal of the ETT may decrease the risk of overall airway complications, including cough and desaturations. However, it may be associated with increased airway obstruction compared with awake extubation in paediatric patients. In our institution, a further technique has become increasingly common practice: removing ETT deep to avoid coughing and desaturation, then inserting a laryngeal mask airway (LMA) which can be removed once the patient is awake in the postoperative care unit (PACU), avoiding the risk of airway obstruction coupled with deep airway removal. The aim of the study is to assess whether deep removal of an ETT and exchange to an LMA, is superior to awake ETT removal with regards to the occurrence of postoperative respiratory adverse events.\n\nIn this study, patients will be randomised to awake removal of ETT or deep removal of an ETT and exchange to an LMA. Data will be collected regarding the rate of respiratory adverse events in either group, as well as the incidence of post-operative pain, delirium and nausea and vomiting.",[82,83,27],"Endotracheal Extubation","Airway Anesthesia",[85,86,87,88,89],"Paediatrics","Anaesthesia","Surgery","Extubation","Respiratory adverse events","RECRUITING","2026-05-28",{"date":93,"type":36},"2026-06-01",{"date":95,"type":36},"2026-02-06",{"date":97,"type":21},"2029-02-28",{"name":99,"class":43},"Telethon Kids Institute",8,{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":109,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":22,"phases":113,"briefSummary":114,"conditions":115,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":4},"100622014","vegetarian-tube-feed-study-100622014","NCT07378111","Vegetarian Tube Feed Study","Acceptability (Including Gastrointestinal Tolerance, Compliance) of a Vegetarian Paediatric Enteral Tube Feed With Food Derived Ingredients.","Tube feed","Inclusion Criteria:\n\n* Patients from 1 -15 years requiring more than 50% of energy from tube feeding or to take alongside home-made blended diet as part of their dietary management for disease related malnutrition.\n* Patients well-established and stable on current nutritional support regimen. Willingly given, written, informed consent from patient\u002Fcaregiver\n\nExclusion Criteria:\n\n* No established tube feed.\n* Inability to comply with the study protocol, in the opinion of the investigator.\n* Under 1 years of age\n* Patients on parenteral nutrition\n* Known food allergies, including to any ingredients listed in appendix 1.\n* Participation in another interventional study within 2 weeks of this study.\n* Patients with known or suspected ileus or mechanical bowel obstruction","1 Year","15 Years",{"count":112,"type":21},25,[24],"This is a single arm, prospective, single-centre study to evaluate the gastrointestinal tolerance and compliance over a 28-day period using a tube feed with food derived ingredients.",[27],"2026-03-11",{"date":118,"type":36},"2026-03-12",{"date":120,"type":21},"2026-03-30",{"date":122,"type":21},"2026-12-22",{"name":124,"class":125},"Société des Produits Nestlé (SPN)","INDUSTRY",{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":131,"acronym":4,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":16,"minAge":133,"maxAge":134,"enrollmentInfo":135,"targetDuration":4,"studyType":137,"phases":4,"briefSummary":138,"conditions":139,"keywords":4,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":154},"100605350","infrared-thermography-for-prediction-of-successful-erector-spinae-plane-block-in-unilateral-inguinal-hernia-surgery-in-paediatric-patients-100605350","NCT07161375","Infrared Thermography for Prediction of Successful Erector Spinae Plane Block in Unilateral Inguinal Hernia Surgery in Paediatric Patients","Infrared Thermography for Prediction of Successful Erector Spinae Plane Block in Unilateral Inguinal Hernia Surgery in Paediatric Patients: A Prospective Observational Study","Inclusion Criteria:\n\n* Age from 3 months to 6 years.\n* Both genders.\n* American Society of Anesthesiologists (ASA) Physical Status I-II.\n* Children undergoing elective unilateral open inguinal hernia surgery.\n\nExclusion Criteria:\n\n* Parents' or guardians' refusal\n* Known Allergy to local anesthetics.\n* Coagulopathy \\[international normalised ratio (INR) \\>1.4 or platelets \\\u003C75.000\\].\n* Infection at the site of injection or wound close to the puncture site.\n* preexisting neuropathy (with sensory and\u002For motor deficits).\n* Diseases interfere with thermal imaging (as skin infections).\n* Baseline oesophageal body temperature of more than 37.5 °C.\n* Emergency and re-do cases will be excluded.","3 Months","6 Years",{"count":136,"type":21},69,"OBSERVATIONAL","This study aims to evaluate the accuracy of temperature change (ΔT) measurements using infrared thermography to predict a successful erector spinae plane block in pediatric patients undergoing inguinal hernia repair under general anesthesia.",[140,141,142,143,144,27],"Infrared","Thermography","Prediction","Erector Spinae Plane Block","Unilateral Inguinal Hernia Surgery","2025-08-30",{"date":147,"type":36},"2025-09-08",{"date":149,"type":36},"2024-08-05",{"date":151,"type":21},"2025-09-01",{"name":153,"class":43},"Cairo University",1,{"id":156,"slug":157,"hasResults":11,"nctId":158,"briefTitle":159,"officialTitle":160,"acronym":161,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":16,"minAge":75,"maxAge":51,"enrollmentInfo":163,"targetDuration":4,"studyType":137,"phases":4,"briefSummary":165,"conditions":166,"keywords":4,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":176,"locationsCount":178},"100569502","nutrition-in-paediatric-critical-care-100569502","NCT06695078","Nutrition in Paediatric Critical Care","Nutrition in Paediatric Critical Care: a Bi-national Prospective Cohort Study","ePICUre","Inclusion Criteria:\n\n1. All patients \\\u003C\u002F=18 years of age\n2. Admitted to the PICU after 00:00 on the day of the study period commencement\n3. Admitted to the PICU for \\>72 hours\n\nExclusion Criteria:\n\n1. Those previously enrolled during the study period (i.e. those re-admitted to PICU)\n2. Those for end of life care only\n3. Those admitted for organ donation",{"count":164,"type":21},200,"This is a multi-centre prospective cohort study of nutrition in paediatric critical care in Australia and New Zealand. The study is planned to run in parallel with the adult ICU cohort study, NUTRIENT. Two study periods are proposed with the first in late 2024 and the second in 2026. This observational study seeks to determine the following (although not limited to) descriptive outcomes of interest:\n\n1. Nutritional outcomes, including route of nutrition support (oral, enteral and\u002For parenteral), energy and protein prescription and provision, and anthropometric measures\n2. Patient-centred outcomes, including duration of invasive respiratory support and hospitalisation, and mortality\n3. Nutrition service delivery in the PICU and ward settings",[167,168,27],"ICU","Nutrition","2024-11-17",{"date":171,"type":36},"2024-11-19",{"date":173,"type":36},"2021-06-07",{"date":175,"type":21},"2027-12",{"name":177,"class":43},"Australian and New Zealand Intensive Care Research Centre",11]