[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"rib-fracture\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:rib-fracture":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,50,76,102],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100635478","spsip-vs-esp-block-for-analgesia-after-rib-fracture-surgery-100635478",false,"NCT07553208","SPSIP vs ESP Block for Analgesia After Rib Fracture Surgery","Ultrasound-guided Serratus Posterior Superior Intercostal Plane Block Versus Erector Spinae Plane Block for Postoperative Analgesia After Surgical Stabilization of Rib Fractures: a Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients aged 18-65 years\n* ASA physical status I-III\n* Scheduled for elective video-assisted thoracoscopic surgery\n* Body mass index (BMI) between 18 and 35 kg\u002Fm²\n* Ability to understand and use the patient-controlled analgesia (PCA) device\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* Refusal to participate\n* Allergy to local anesthetics\n* Infection at the injection site\n* Coagulopathy or ongoing anticoagulant therapy\n* Chronic opioid use or opioid dependence\n* Severe hepatic or renal insufficiency\n* Pregnancy or breastfeeding\n* Cognitive impairment or inability to communicate pain scores\n* Body mass index (BMI) \\\u003C18 or \\>35 kg\u002Fm²","ALL","18 Years","65 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Serratus Posterior Superior Intercostal Plane (SPSIP) block and the Erector Spinae Plane (ESP) block in patients undergoing surgical stabilization of rib fractures. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block performance time, block-related and systemic side effects (hematoma, pneumothorax, local anesthetic systemic toxicity, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, and quality of recovery assessed using the QoR-15 questionnaire.",[27,28,29],"Rib Fracture","Postoperative Pain","Thoracic Trauma",[31,32,33,34,35,36],"serratus posterior superior intercostal plane block","spsıp block","erector spine plane block","esp","rib fixation","regioanl anethesia","NOT_YET_RECRUITING","2026-05-07",{"date":40,"type":41},"2026-05-11","ACTUAL",{"date":43,"type":21},"2026-11-15",{"date":45,"type":21},"2028-06-15",{"name":47,"class":48},"Antalya City Hospital","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100618976","point-of-care-ultrasound-pocus-for-diagnosis-and-treatment-of-fractures-in-the-costal-cartilage-100618976","NCT07338617","Point of Care Ultrasound (POCUS) for Diagnosis and Treatment of Fractures in the Costal Cartilage","Inclusion Criteria:\n\n* Trauma patients (≥18 years) treated at the Department of Surgery, Sahlgrenska University Hospital, where CT has shown at least one recent injury to the chest wall.\n\nExclusion Criteria:\n\n* Patients with injuries resulting from CPR, severe head injury, spinal injury, and neurological or musculoskeletal disease affecting chest mobility will be excluded.",{"count":57,"type":21},100,"OBSERVATIONAL","The goal of this observational study is to learn if combining ultrasound and CT scans can better diagnose cartilage fractures in the ribs, and to understand how finding these injuries affects treatment decisions for patients with injuries to the Chest wall.\n\nThe main questions it aims to answer are:\n\n* Does using both ultrasound and CT scans find more costal cartilage fractures than CT scans alone?\n* Does discovering costal cartilage fractures change how patients are treated, such as whether more patients receive surgery or if different fractures are repaired?\n* How do costal cartilage fractures heal, and do they affect lung function, pain, or the risk of complications after surgery?\n\nPatients with cartilage injuries will be followed up at 1, 3, and 12 months after their injury. They will be checked for pain, instability, and healing using ultrasound and sometimes CT scans. The study will also assess lung function, quality of life, and pain levels.",[27,61],"Cartilage Damage",[63,64,65,66],"Rib Fractures","Fractures, Cartilage","Ultrasonography","Traumatology","2026-04-27",{"date":69,"type":41},"2026-04-28",{"date":71,"type":21},"2026-06",{"date":73,"type":21},"2028-01",{"name":75,"class":48},"Sahlgrenska University Hospital",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":83,"targetDuration":85,"studyType":58,"phases":4,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":49},"100630296","zimmer-biomet-ribfix-titan-100630296","NCT07485829","Zimmer Biomet-RibFix Titan","Zimmer Biomet Patient Outcomes and Experience After Chest Wall Repair With RibFix Titan™","Inclusion Criteria:\n\n1. At least 18 years of age\n2. Willing and able to sign an Institutional Review Board (IRB) approved Informed Consent Form and able to comply with study requirements, in the Investigator's opinion\n3. Independent of study participation, patient qualifies for fixation, stabilization, and\u002For fusion of rib fractures or osteotomies of normal and osteoporotic bone with the study device\n\nExclusion Criteria:\n\n1. Midline Sternotomy: sternotomy incisions crossing the midline\n2. Active Infection: patients should not have any ongoing infections\n3. Material Sensitivity: where sensitivity to materials is suspected, comprehensive testing should be conducted before implantation\n4. Inability to Adhere to Post-operative Care: Patients must have the ability and willingness to comply with post-operative care instructions, which may not be possible for individuals with certain mental or neurological conditions\n5. Patients not expected to survive the duration of follow-up due to the involvement of trauma situations\n6. Patients with a history of alcohol or substance abuse, as well as vulnerable populations such as prisoners and pregnant women",{"count":84,"type":21},54,"1 Year","Prospective, single-center, non-randomized, single-cohort, post-market clinical follow-up study to confirm the safety, performance, and clinical benefits for the use of the RibFix Titan™ system implants and instrumentation) in the fusion, stabilization, and fixation of fractures in the chest wall including rib reconstructive surgical procedures, trauma, or planned osteotomies.",[27,88],"Rib Fracture Multiple",[90],"RibFix Titan","RECRUITING","2026-04-15",{"date":94,"type":41},"2026-04-21",{"date":96,"type":41},"2026-03-31",{"date":98,"type":21},"2028-03",{"name":100,"class":101},"Zimmer Biomet","INDUSTRY",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":109,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":112,"conditions":113,"keywords":115,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":125},"100450553","ribfix-blu-thoracic-fixation-system-versus-non-surgical-treatment-in-non-flail-chest-rib-fractures-100450553","NCT05146986","RibFix Blu Thoracic Fixation System Versus Non-surgical Treatment in Non-flail Chest Rib Fractures","Prospective Multi-center Comparative Study of RibFix Blu Thoracic Fixation System Versus Non-surgical Treatment in Non-flail Chest Rib Fractures","Inclusion Criteria:\n\n* Age 18 and above (inclusive)\n* Simple rib fracture with ≥ 3 consecutive ribs, and the broken ends showed clear displacements\n* Indicated for surgical repair of rib fractures using RibFix Blu Thoracic Fixation System or non-surgical treatment (analgesia and symptomatic management treatment)\n* Willing and able to complete scheduled follow-up evaluations as described in the study protocol\n* Has participated in the Informed Consent process and is willing and able to sign an Institutional Review Board or Ethics Committee (IRB\u002FEC) approved Patient Information\u002F Informed consent Form (PICF)\n\nExclusion Criteria:\n\n* Flail chest rib fractures based on radiological or clinical findings\n* Previous rib fractures or pulmonary problems, requiring continuous oxygen use at home pre-trauma\n* Presence of any serious medical issues that placed patient in generally poor conditions such that he or she could not tolerate the surgery\n* Chest trauma associated with severe craniocerebral injury, abdominal organ injury, severe spinal injury, limb fracture, or pelvic fracture requiring long-term bed rest\n* Has serious medical disease that is a contraindication for general anesthesia, such as cerebral infarction, myocardial infarction and hemorrhagic syndrome\n* Any contraindications listed in the manufacturer's Instruction to use for RibFix Blu Thoracic Fixation System as per below:\n\n  * Spanning a midline sternotomy\n  * Active Infection\n  * Foreign body sensitivity\n* Is known to be pregnant\n* Is a prisoner, known alcohol or drug user or mentally incompetent or unable to understand what participation in this study entails.\n* Participation in another surgical intervention that may influence any of the outcome parameters.",true,{"count":111,"type":21},167,"This is a prospective, multi-center, observational, cohort study involving skilled cardiothoracic surgeons who are experienced in implanting the treatment of non-flail chest rib fractures and the use of RibFix Blu Thoracic Fixation System.",[114],"Rib; Fracture",[116],"Non-flail chest","2024-03-05",{"date":119,"type":41},"2024-03-07",{"date":121,"type":41},"2022-01-02",{"date":123,"type":21},"2026-12-30",{"name":100,"class":101},5]