[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"birth-preterm\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:birth-preterm":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100651024","the-neu---cap-trial-100651024",false,"NCT07754032","The NEU - CAP Trial","A Randomised Trial of Colorimetric Carbon Dioxide (CO₂) Detector-guided Non-invasive Ventilation Versus Standard Care: The NEU-CAP Trial","NEU-CAP","Inclusion Criteria:\n\n* Born before 32 weeks of gestation\n* Received non-humidified face-mask support in the first 10 minutes of life\n* Parental consent obtained\n\nExclusion Criteria:\n\n* Congenital diaphragmatic hernia\n* Tracheo-oesophageal fistula\n* Cyanotic heart disease\n* Surfactant protein deficiency\n* Any other congenital abnormality or condition with an adverse effect on breathing, ventilation, or oxygenation. Many of the infants enrolled in the study will later be diagnosed with respiratory distress syndrome (RDS); this will not render them ineligible for inclusion.","ALL","32 Weeks",{"count":20,"type":21},1860,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of NEU-CAP is to investigate the clinical impact of using a colorimetric carbon dioxide (CO₂) detector during non-invasive ventilation (NIV). Infants born before 32 weeks of gestation will be included in this trial. This is a stepped-wedge cluster randomised controlled trial. The participating centre, rather than the individual infant, will be the unit of randomisation. This design is appropriate to test the effect of an intervention that encompasses a behavioural aspect, in this case CO₂-detector-guided non-invasive ventilation.",[27,28,29],"Infant, Premature, Diseases","Birth, Preterm","Respiratory Distress Neonatal",[31,32,33,34],"Resuscitation","Preterm infant","Non-invasive ventilation","CO₂-detection","NOT_YET_RECRUITING","2026-08-06",{"date":38,"type":39},"2026-08-10","ACTUAL",{"date":41,"type":21},"2027-01",{"date":43,"type":21},"2028-03",{"name":45,"class":46},"Leiden University Medical Center","OTHER",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":18,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100511706","the-neu-stim-trial-100511706","NCT05942924","The NEU-STIM Trial","A Randomised Trial of Repetitive Versus Selective Tactile Stimulation for Preterm Infants at Birth: The NEU-STIM Trial","NEU-STIM","Inclusion Criteria:\n\n* Infants born before 32 weeks of gestation can be included in this trial after parental consent.\n\nExclusion Criteria:\n\n* Infants will be excluded if they are found to have a congenital abnormality or condition that has an adverse effect on breathing\u002Fventilation or oxygenation, including: congenital diaphragmatic hernia, trachea-oesophageal fistula, cyanotic heart disease and surfactant protein deficiency. Many of the infants enrolled in the study will later be diagnosed with respiratory distress syndrome (RDS); this will not render them ineligible for inclusion.",{"count":56,"type":21},3280,[24],"The aim of this study is to determine the effect of repetitive tactile stimulation compared to selective stimulation on oxygenation of the infant at 5 minutes after birth. Infants born before 32 weeks of gestation will be included in this trial. This is a stepped-wedge cluster randomised controlled trial. The participating centre, rather than the individual infant, will be the unit of randomisation. This design is appropriate to test the effect of an intervention that encompasses a behavioral aspect - in this case the performance of tactile stimulation.",[27,28],[32,61,31],"Tactile stimulation","RECRUITING","2025-03-05",{"date":65,"type":39},"2025-03-10",{"date":67,"type":39},"2024-03-11",{"date":69,"type":21},"2025-12-31",{"name":45,"class":46},43]