[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pectus-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pectus-surgery":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100641693","long-term-safety-of-preoperative-percutaneous-intercostal-cryoneurolysis-100641693",false,"NCT07657845","Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis","Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis: Neuropathic Pain, Quality of Life and Sensory Recovery in a Paediatric Cohort Following Pectus Excavatum Repair","CRYOFUP","Inclusion Criteria:\n\n* Patients who underwent percutaneous cryoneurolysis.\n* Patients who underwent surgical correction of pectus excavatum according to the Nuss procedure.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Peripheral nervous system disorders\n* Age \\\u003C 14 years\n* Failure to attend scheduled follow-up visits","ALL","14 Years",{"count":20,"type":21},50,"ESTIMATED","OBSERVATIONAL","Follow up of patients who underwent percutaneous cryoneurolysis for pectus excavatum repair (the Nuss procedure) pain management",[25,26],"Cryo Analgesia","Pectus Surgery",[28,29,30,31,32,33,34,35],"follow up","lanss","neuropathy","chronic pain","cpsp","neuropathic pain","sensitivity recovery","PedsQL","RECRUITING","2026-06-17",{"date":39,"type":40},"2026-06-22","ACTUAL",{"date":42,"type":40},"2025-02-02",{"date":44,"type":21},"2029-01-15",{"name":46,"class":47},"Papa Giovanni XXIII Hospital","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":73,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":48},"100523273","studying-melatonin-and-recovery-in-teens-100523273","NCT06093477","Studying Melatonin and Recovery in Teens","SurgerySMART: Studying Melatonin and Recovery in Teens","SurgerySMART","Inclusion Criteria:\n\nPatients\u002Fyouth:\n\n* Age 12-18 years\n* Participants undergoing elective major musculoskeletal surgery for eligible conditions\n* California state resident\n* Regular access to internet and smartphone\n* Can read and understand English or Spanish\n\nParents\u002Fcaregivers\n\n* Biological parent or legal guardian of youth\n* Can read and understand English or Spanish\n\nExclusion Criteria:\n\nPatients\u002Fyouth\n\n* Prescription medication for premorbid insomnia\n* Cognitive impairment or developmental delay\n* Does not agree to a 1-week washout if taking over the counter supplements or other sleep aids prior to the start of the study medication\n* High risk for sleep related breathing disorder\n* Chronic medical condition that is severe\u002Fsystemic or requires regular treatment regimen\n* Psychiatric admission in prior 30 days\n* Patients that underwent major surgery in the last 3 months, or those that have not fully recovered from a prior surgery\n* BMI ≥ 99th percentile\n* Enrollment in another therapeutic study\n* Any serious underlying medical or psychiatric condition, that, in the opinion of the investigator, would contraindicate the patient's participation in the study","12 Years","18 Years",{"count":60,"type":21},45,"INTERVENTIONAL",[63],"NA","The goal of this feasibility clinical trial is to learn if melatonin can help teens having major musculoskeletal surgery by promoting healthy sleep. Melatonin is available as a dietary supplement that may be effective in promoting longer, higher quality sleep. This study will assess the feasibility and acceptability of melatonin for teens undergoing major musculoskeletal surgery, as well as determine optimal measured outcomes (sleep, pain, health-related quality of life) at short- and long-term follow-up.",[66,67,68,69,70,71,26,72],"Juvenile; Scoliosis","Scoliosis Idiopathic","Scoliosis; Adolescence","Scoliosis;Congenital","Kyphosis","Spondylolisthesis","Hip Surgery",[74,75,76,77,78,79,31,80,81,82,83,84,85,86],"sleep","pain medicine","pediatric pain medicine","melatonin","pilot feasibility trial","acute pain","CPSP","chronic postsurgical pain","spinal fusion surgery","adolescent","perioperative melatonin","hip surgery","pectus surgery","2026-03-16",{"date":89,"type":40},"2026-03-18",{"date":91,"type":40},"2024-05-30",{"date":93,"type":21},"2028-03-31",{"name":95,"class":47},"Stanford University"]