[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"drowning-anoxia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:drowning-anoxia":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,33],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":16,"enrollmentInfo":4,"targetDuration":4,"studyType":17,"phases":4,"briefSummary":18,"conditions":19,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":4,"completionDateStruct":4,"leadSponsor":30,"locationsCount":5},"100310906","expanded-access-protocol-umbilical-cord-blood-infusions-for-children-with-brain-injuries-100310906",false,"NCT03327467","Expanded Access Protocol: Umbilical Cord Blood Infusions for Children With Brain Injuries","Under this protocol, participants may be eligible for infusion of autologous, sibling, and\u002For unrelated donor CB cells (Duke only). Some eligibility criteria vary based on CB source. For all participants, eligibility is predicated on the availability of a qualifying CB unit To be eligible, patients must:\n\nInclusion Criteria:\n\n1. Age at Consent:\n\n   1. Autologous: 0-26 years\n   2. Sibling: 6 months - 26 years\n   3. Unrelated Donor (Duke only): 6 months - 26 years\n2. Diagnosis\n\n   1. Autologous and Sibling: Cerebral palsy, Hypoxic brain injury, Stroke, Hydrocephalus, Apraxia (without autism), Other brain injury\n   2. Unrelated Donor (Duke only): Motor impairment secondary to: Hypoxic brain injury, Periventricular leukomalacia, Stroke\u002Fbleed, Congenital hydrocephalus\n3. Functional Status:\n\n   1. Autologous and Sibling: See exclusion criteria\n   2. Unrelated Donor (Duke only): GMFCS level I-IV (age ≥2)\n4. No clinically significant abnormalities in blood counts and basic chemistries for age.\n5. Absolute Lymphocyte Count:\n\n   * 1200 for African American participants\n   * 1500 for all other participants\n6. Availability of a qualified autologous or Sibling CB Unit\n\n   1. Autologous or Sibling: available\n   2. Unrelated Donor (Duke only): N\u002FA\n7. Written informed consent obtained from the parent or legal guardian.\n\nExclusion Criteria:\n\n1. Documented HIV or Hepatitis or other disease transmittable through the blood.\n2. A cord blood unit that fails to meet specifications\n3. Refusal of consent\n4. Uncontrolled seizure disorder\n5. Uncontrolled infection\n6. Diagnosed with a genetic or metabolic disorder related to the neurologic condition\n7. History of an immune deficiency\n8. History of treatment with chemo or immunosuppressive therapy\n9. History of previous allogeneic cell therapy outside of participation in a Duke clinical trial\n10. Need for mechanical ventilation or chronic O2 support\n11. Unstable airway\n12. Eligible for an active clinical trial of cellular therapy at Duke. If previously enrolled on another Duke cell therapy protocol the participant may still be considered for enrollment on this study after the follow-up period for the clinical trial is completed.\n13. Cerebral palsy secondary to infection, congenital or otherwise, without another known cause\n14. Pregnant or breastfeeding\n15. Treated with autologous cellular therapy through a non-intravenous route (ie. intrathecally) within one year prior to enrollment.\n\nUmbilical Cord Blood Criteria\n\nParticipant enrollment is dependent on the availability of a banked unit of autologous or sibling CB that has been stored at a private or public bank, or, if enrolling at Duke, availability of a publicly banked unrelated donor unit. Units must meet the following criteria:\n\nPrecryopreservation:\n\n1. TNCC ≥2x107\u002Fkg\n2. Sterility cultures performed and negative\n3. Viability ≥70%\n4. At least haploidentical HLA match for sibling units and at least a 4\u002F6 HLA match for unrelated donor units\n5. Donor screening testing performed and negative\n\nCBU Test sample\n\n1. Segment or test vial available\n2. Identity confirmed via HLA typing of test sample and donor\n3. Viability testing recommended, but not required","ALL","26 Years","EXPANDED_ACCESS","This protocol is designed to enable access to intravenous infusions of banked umbilical cord blood (CB), that is thawed and not more than minimally manipulated, for children with various brain disorders. Children with cerebral palsy, congenital hydrocephalus, apraxia, stroke, hypoxic brain injury and related conditions will be eligible if they have normal immune function and do not qualify for, have previously participated in, or are unable to participate in an active cell therapy clinical trial at Duke Medicine. For the purpose of this protocol the term children refers to patients less than 26 years of age. Cord blood is administered as a cellular infusion without prior treatment with chemotherapy or immunosuppression. The mechanism of action is through paracrine signaling of cord blood monocytes inducing endogenous cells to repair existing damage.",[20,21,22,23,24],"Cerebral Palsy","Hydrocephalus","Apraxia of Speech","Hypoxia Ischemia, Cerebral","Drowning; Anoxia","AVAILABLE","2026-01-22",{"date":28,"type":29},"2026-01-23","ACTUAL",{"name":31,"class":32},"Joanne Kurtzberg, MD","OTHER",{"id":34,"slug":35,"hasResults":11,"nctId":36,"briefTitle":37,"officialTitle":38,"acronym":39,"eligibilityCriteria":40,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":41,"targetDuration":4,"studyType":44,"phases":4,"briefSummary":45,"conditions":46,"keywords":58,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100539949","the-emergency-call-on-drowning-100539949","NCT06310486","The Emergency Call on Drowning","The Emergency Call on Drowning: A Registry-based Cohort Study of the Characteristics, Predictors, and Outcomes of Fatal and Non-fatal Drowning","DROWN_CALL","Inclusion Criteria:\n\n* Patients at all ages registered in the Danish Prehospital Drowning Data are eligible.\n\nExclusion Criteria:\n\n* Obvious clinical signs of irreversible death (decapitation, decomposition, post-mortem lividity, post-mortem rigidity)\n* A valid Do-Not-Attempt-Resuscitation (DNAR) order or other code status orders limiting life-sustaining therapies\n* Missing or corrupted audio files\n* Missing identification number\n* Missing 30-day survival",{"count":42,"type":43},1500,"ESTIMATED","OBSERVATIONAL","This study aims to 1) describe patient-, setting-, and dispatcher-related characteristics in drowning-related emergency calls to the Emergency Medical Dispatch Centre (1-1-2 emergency phone) and 2) factors associated with 30-day survival. The investigators will separately analyse drowning-related out-of-hospital cardiac arrest (OHCA) and drowning-related non-OHCA. If feasible, the investigators will qualitatively analyse the calls to identify and describe potential barriers for an optimal handling strategy.",[47,24,48,49,50,51,52,53,54,55,56,57],"Drowning","Drowning, Near","Drowning; Asphyxia","Drowning and Nonfatal Submersion","Drowning or Immersion of Unknown Intent","Drowning and Submersion, Undetermined Intent","Drowning and Submersion While in Bath-Tub","Drowning and Submersion While in Natural Water","Drowning and Submersion Due to Sailboat Sinking","Drowning and Submersion Due to Fall Off Ship","Drowning and Submersion While in Swimming-Pool",[59,47,60,61,62,63,64,65,66,67,68,69],"Emergency Medical Service (EMS)","Emergency Medical Dispatch Centre","Emergency Medical Coordination Centre","Dispatch","Emergency Call","Registry","Database","Epidemiology","Danish Drowning Formula","Danish Prehospital Drowning Data","Utstein","RECRUITING","2025-06-01",{"date":73,"type":29},"2025-06-04",{"date":75,"type":29},"2016-01-01",{"date":77,"type":43},"2025-12-31",{"name":79,"class":32},"Prehospital Center, Region Zealand",1]