[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100587556":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":36,"locations":45,"responsibleParty":88,"collaborators":26,"id":90,"slug":91,"hasResults":92,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":26,"eligibilityCriteria":96,"healthyVolunteers":92,"sex":97,"minAge":98,"maxAge":99,"enrollmentInfo":100,"targetDuration":26,"studyType":103,"phases":104,"briefSummary":106,"conditions":107,"keywords":109,"overallStatus":48,"whyStopped":26,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":121},{"fullName":5,"class":6},"TecTraum Inc.","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Pro2Cool intervention with standard of care","EXPERIMENTAL","The treatment arm will receive standard of care for concussion along with 30 minutes of headneck cooling in the clinic while being monitored for side effects. The Pro2Cool® will be used to provide head and neck cooling.",[13],"Device: Pro2Cool Device",{"label":15,"type":16,"description":17,"interventionNames":18},"Sham Pro2Cool with standard of care","SHAM_COMPARATOR","The control arm will receive standard of care like the treatment group, along with 30 minutes of sham Pro2Cool® placement in the clinic while being monitored for side effects. The Pro2Cool® device will not be used to provide neck cooling; a sham cooling garment device will be placed with impaired cooling function (only to the head), with sham treatment temperature being set to 19°C (instead of the therapeutic 6°C specification).",[19],"Device: Sham Cooling Garment Device",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Pro2Cool Device","The Pro2Cool Device is a non-invasive hypothermic therapy (\"cold therapy\") device that provides localized cooling of the head and neck. Water and isopropyl alcohol cooled to 6°C by the chiller assembly circulate through the cooling garment to create conductive heat transfer from the scalp and carotid arteries, thus achieving cooling of the brain.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Sham Cooling Garment Device","The sham cooling garment device will be placed with impaired cooling function (only to the head), with sham treatment temperature being set to 19°C (instead of the therapeutic 6°C specification). There will be no thermal nylon barrier that will be used and flow to the neck bladder will be closed.",[15],[32],{"name":33,"affiliation":34,"role":35},"Brian Reilly, MD","Children's Hospital Medical Center of Akron","PRINCIPAL_INVESTIGATOR",[37,42],{"name":38,"role":39,"phone":40,"phoneExt":26,"email":41},"John Zak, MD, MBA","CONTACT","216-789-7676","jzak@tectraum.com",{"name":43,"role":39,"phone":26,"phoneExt":26,"email":44},"Rebecca Zickert","rebecca.zickert@brightresearch.com",[46,63,75],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"University of Michigan","RECRUITING","Ann Arbor","Michigan","48109","United States","US",{"type":55,"coordinates":56},"Point",[57,58],-83.74088,42.27756,{"lat":58,"lon":57},[61],{"name":62,"role":35,"phone":26,"phoneExt":26,"email":26},"Ingrid Ichesco, MD",{"facility":64,"status":48,"city":65,"state":66,"zip":67,"country":52,"countryCode":53,"cosmosGeoPoint":68,"geoPoint":72,"contacts":73},"Akron Children's Hospital","Akron","Ohio","44308",{"type":55,"coordinates":69},[70,71],-81.51901,41.08144,{"lat":71,"lon":70},[74],{"name":33,"role":35,"phone":26,"phoneExt":26,"email":26},{"facility":76,"status":77,"city":78,"state":66,"zip":79,"country":52,"countryCode":53,"cosmosGeoPoint":80,"geoPoint":84,"contacts":85},"Cleveland Clinic Foundation","NOT_YET_RECRUITING","Cleveland","44125",{"type":55,"coordinates":81},[82,83],-81.69541,41.4995,{"lat":83,"lon":82},[86],{"name":87,"role":35,"phone":26,"phoneExt":26,"email":26},"Sami Rifat, MD",{"type":89,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100587556","pro-2-cool-pivotal-trial-ii-100587556",false,"NCT06929923","Pro-2-Cool Pivotal Trial II","A Double-Blind, Randomized Study of Clinical Efficacy of Hypothermic Therapy Following Concussion in Adolescent Athletes as Compared to a Sham-Controlled Population","Inclusion Criteria:\n\n1. Males and females, 13-21 years of age\n2. Confirmed concussion diagnosis consistent with American Congress Rehabilitation Medicine guidelines 21, without any of the following:\n\n   * Glasgow Coma Scale (GCS) score of less than 13 at 30 minutes post-injury\n   * Loss of consciousness greater than 30 minutes\n   * Post-traumatic amnesia lasting over 24 hours\n3. Glasgow Coma Scale (GCS) ≥ 13 at the time of initial injury for study enrollment.\n4. Post-Concussion Symptom Scale Score minimum of 15\n5. Initial provider visit is within 7 days of injury\n6. In generally good health as confirmed by medical history and determined by site investigator or designated trained healthcare professional under the supervision of the principal investigator.\n7. Has informed consent obtained per protocol and as required per Institutional Review Board\n\nExclusion Criteria:\n\n1. Age \\\u003C 13 years or \\> 21 years\n2. Inability to understand the study requirements or provide informed consent\n3. Cleared to return to play during initial visit\n4. Prior participation in a Pro2Cool Clinical Study\n5. Serious traumatic brain injury as evidenced by worsening symptoms:\n\n   * Vomiting \\> 2 episodes following injury\n   * Seizure\n   * Hospitalization\n   * Radiology scan indicating brain bleed\n   * Slurred speech which has not resolved within 72 hours of concussive injury\n6. Physical (e.g., head or neck injury that requires medical treatment) or mental disability hindering adequate response to assessment of symptoms\n7. Hemodynamic instability\u002Fmedical condition requiring further acute life-saving medical intervention\n8. History of psychiatric disorder that includes suicide attempts within the last 6 months, unmanaged depression or anxiety, hospitalization for psychiatric treatment within the last 6 months\n9. Known brain mass, intracranial hemorrhage, skull fracture\n10. Scalp abnormalities including laceration or bleeding\n11. Presence of ventriculoperitoneal (VP) shunt\n12. Known hematological malignancies, including, but not limited to: multiple myeloma, leukemia, and lymphoma\n13. Known history of Reynaud's Disease compromised liver function, cold agglutination, cold sensitivity, cryoglobulinemia, cryofibrinogenemia, and\u002For a history of severe migraines\n14. Known or disclosed pregnancy or breast-feeding\n15. Sustains another head or neck injury at the time of concussive injury which requires medical treatment","ALL","13 Years","21 Years",{"count":101,"type":102},66,"ESTIMATED","INTERVENTIONAL",[105],"NA","This study is being conducted to determine the clinical safety and efficacy of Pro-2-Cool mediated head and neck cooling when applied after concussion and improved symptomatology among adolescent athletes as quantified by post-concussion symptom severity (PCSS) score.",[108],"Concussion, Mild",[110,111],"Non-invasive hypothermic therapy","Sports-related concussion","2026-06-09",{"date":114,"type":115},"2026-06-11","ACTUAL",{"date":117,"type":115},"2025-02-20",{"date":119,"type":102},"2027-06",{"name":5,"class":6},3]