[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pediatric-surgical-procedures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pediatric-surgical-procedures":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,78],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100562847","a-study-of-harmonic-700-shears-with-advanced-hemostasis-in-pediatric-and-adult-surgical-procedures-100562847",false,"NCT06608485","A Study of HARMONIC 700 Shears With Advanced Hemostasis in Pediatric and Adult Surgical Procedures","A Prospective, Single-Arm Multi-Center Study of the HARMONIC™ 700, 5 mm Diameter Shears With Advanced Hemostasis in Pediatric Surgical Procedures (General) and Adult Surgical Procedures (General, Gynecological, Urological, and Thoracic)","Inclusion Criteria:\n\nPediatric participants\n\n* Non-emergent procedure (general) where at least one vessel is planned to be transected by the HARMONIC 700 Shears per the IFU\n* Less than 18 years of age at the time of procedure\n* Participant's parent\u002Flegal guardian must give permission to participate in the study and provide written informed consent for the participant Adult participants\n* Elective procedure (general, gynecological, urological, or thoracic) where at least one vessel is planned to be transected by the HARMONIC 700 Shears per the IFU\n* Elective procedure (general, gynecological, urological, or thoracic) where at least one vessel is planned to be transected by the HARMONIC 700 Shears per the IFU\n\nExclusion Criteria:\n\nPreoperative\n\n* Physical or psychological condition which would impair study participation\n* Participants of childbearing potential who are pregnant\n* Enrollment in a concurrent interventional clinical study that could impact the study endpoints Intraoperative\n* HARMONIC 700 Shears were not attempted to be used for at least one single vessel transection during the surgical procedure","ALL","110 Years",{"count":19,"type":20},165,"ESTIMATED","OBSERVATIONAL","The main purpose of this study is to demonstrate acceptable performance and assess safety of the HARMONIC 700 Shears device in a post-market setting when used per the instructions for use in pediatric and adult surgical procedures.",[24,25,26,27,28],"Pediatric Surgical Procedures","Adult Surgical Procedures","Adult Gynecological Procedures","Adult Urological Procedures","Adult Thoracic Procedures","RECRUITING","2026-06-04",{"date":32,"type":33},"2026-06-05","ACTUAL",{"date":35,"type":33},"2025-01-23",{"date":37,"type":20},"2026-08-15",{"name":39,"class":40},"Ethicon Endo-Surgery","INDUSTRY",9,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":54,"studyType":21,"phases":4,"briefSummary":55,"conditions":56,"keywords":61,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":77},"100611562","transversalis-fascia-plane-versus-transversus-abdominis-plane-block-for-postoperative-analgesia-in-children-100611562","NCT07242196","Transversalis Fascia Plane Versus Transversus Abdominis Plane Block for Postoperative Analgesia in Children","Comparison of the Analgesic Effects of Ultrasound-Guided Transversalis Fascia Plane Block and Transversus Abdominis Plane Block in Pediatric Laparoscopic Surgery","Inclusion Criteria:\n\n* Pediatric patients aged 6 months to 16 years\n* Classified as ASA physical status I or II\n* Scheduled to undergo laparoscopic surgery under general anesthesia\n\nExclusion Criteria:\n\n* Patients classified as ASA physical status III or IV\n* Known allergy or hypersensitivity to local anesthetic agents\n* Presence of bleeding diathesis or coagulation disorders\n* Infection at the injection site or local skin lesions preventing block application",true,"6 Months","16 Years",{"count":53,"type":20},36,"1 Day","This prospective clinical study aims to compare the postoperative analgesic efficacy of the ultrasound-guided transversalis fascia plane block (TFPB) and the transversus abdominis plane (TAP) block in pediatric patients undergoing laparoscopic surgery. Effective and long-lasting postoperative analgesia is essential for patient and parental satisfaction in pediatric anesthesia. With recent advances in ultrasound technology, regional anesthesia techniques have become increasingly utilized in pediatric practice.\n\nIn the TAP block, local anesthetic is injected between the internal oblique and transversus abdominis muscles, providing analgesia typically between Torachal vertebra 10 (T10) and Lumbar vertebra (L1) dermatomes. The transversalis fascia plane block, developed as a modification of this approach, targets the proximal portions of the T12 and L1 nerves by depositing local anesthetic between the transversus abdominis muscle and the transversalis fascia, potentially offering wider sensory coverage.\n\nThis study compares both blocks in terms of postoperative pain scores, duration of analgesia, and requirement for rescue analgesics in children undergoing laparoscopic surgery. The results are expected to contribute to the optimization of regional anesthesia techniques and improve pain management strategies in pediatric surgical patients.",[57,58,59,24,60],"Postoperative Analgesia","Transversus Abdominis Plane (TAP) Block","Transversalis Fascia Plane Block","Laparoscopic Abdominal Surgeries",[62,63,64,65,66],"transversus abdominis plane block","transversalis fascia plane block","pediatrics","laparoscopic abdominal surgery","postoperative analgesia","2026-03-09",{"date":69,"type":33},"2026-03-10",{"date":71,"type":33},"2025-12-18",{"date":73,"type":20},"2026-06-15",{"name":75,"class":76},"Sakarya University","OTHER",1,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":89,"phases":90,"briefSummary":92,"conditions":93,"keywords":94,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":5},"100592303","adolescent-surgery-roadmap-feasibility-and-acceptability-study-100592303","NCT06991673","Adolescent Surgery Roadmap Feasibility and Acceptability Study","Ane-Roadmap","Inclusion Criteria (Adolescent Patient):\n\n* Patient is aged 12-17 years on the date of surgery\n* Surgery is a scheduled surgery (non-emergency)\n* Surgery is occurring within the University of Michigan hospital system (University Hospital, C.S. Mott Children's Hospital, Brighton Ambulatory Surgery Center, East Ann Arbor Ambulatory Surgery Center)\n* Participants are able to enroll within 1-2 weeks of surgery\n* Patient and caregiver must be willing to participate\n* Adolescent and caregiver must have a compatible smartphone and\u002For tablet with internet access and be willing to download an app\n* Eligible patient is able to sign\u002Fassent form\n* Adolescent-caregiver dyad has at least one risk factor for adverse post-operative pain outcomes based on pre-enrollment screening (e.g., worries about managing pain, return to normal activities, limitations in doing desired activities, trouble with sleep)\n\nInclusion Criteria (Caregiver):\n\n* Patient and caregiver must be willing to participate\n* Caregiver must be providing at least 50% of the patient's postsurgical caregiving\n* Caregivers agree to provide informed consent that is in regulatory compliance and IRBMED-approved and also in accordance with institutional guidelines\n* Adolescent and caregiver must have a compatible smartphone and\u002For tablet with internet access and be willing to download an app\n\nExclusion Criteria (Adolescent Patient):\n\n* Adolescent or caregiver are unable to complete intervention activities or surveys in spoken or written English\n* Significant developmental delay, making it impossible for the participant to use an app to complete interventions or answer survey questions\n* Foster children or wards of the state are not eligible for inclusion\n* Hardware removal or debridement surgery (not considered as painful as other orthopedic surgeries)\n* Scoliosis surgery (due to extended longitudinal relationship with surgeon)\n* Concurrent participation in another behavioral\u002Fself-management intervention trial\n* Any impairment, activity, or situation that in the judgment of the Study Coordinator or Principal would make it inappropriate for the subject to participate\n\nExclusion Criteria (Caregiver):\n\n* Significant developmental delay, making it impossible for the participant to use an app to complete interventions or answer survey questions\n* Adolescent or caregiver are unable to complete intervention activities or surveys in spoken or written English\n* Any impairment, activity, or situation that in the judgment of the Study Coordinator or Principal would make it inappropriate for the subject to participate","12 Years","99 Years",{"count":88,"type":20},100,"INTERVENTIONAL",[91],"NA","The goal of this clinical trial is to test the feasibility and acceptability of using a mobile health app, Ane-Roadmap, designed to support adolescents (ages 12-17) undergoing painful surgeries and their caregivers. The main questions it aims to answer are:\n\n* Can adolescent surgery patients and their caregivers be successfully enrolled in the study, with at least 40% of those invited choosing to participate?\n* Will participants actively use the mobile app, completing at least two activities per week for at least half of the study period, either individually and\u002For as a caregiver-adolescent pair?\n\nParticipants will:\n\n* Use the Ane-Roadmap app during their post-surgery recovery period to complete resilience-building activities aimed at improving wellbeing\n* Use the app either individually or together as a caregiver-adolescent pair.\n* Complete surveys regarding risk factors for adverse postsurgical pain outcomes and physical and psychological symptoms experienced postoperatively\n* Some participants will complete a semi-structured interview in which experiences with the study and intervention activities will be elicited",[24],[95,96,97,98,99,100,101,102],"positive psychology","mobile health","surgical recovery","adolescent","caregiver","pediatric surgery","mobile health intervention","positive psychology intervention","NOT_YET_RECRUITING","2025-06-02",{"date":106,"type":33},"2025-06-05",{"date":108,"type":20},"2025-07",{"date":110,"type":20},"2029-12",{"name":112,"class":76},"University of Michigan"]