[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100538616":3},{"organization":4,"armGroups":7,"interventions":26,"overallOfficials":44,"centralContacts":49,"locations":57,"responsibleParty":101,"collaborators":104,"id":108,"slug":109,"hasResults":110,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":114,"eligibilityCriteria":115,"healthyVolunteers":110,"sex":116,"minAge":117,"maxAge":32,"enrollmentInfo":118,"targetDuration":32,"studyType":121,"phases":122,"briefSummary":124,"conditions":125,"keywords":128,"overallStatus":90,"whyStopped":32,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":137,"completionDateStruct":139,"leadSponsor":141,"locationsCount":142},{"fullName":5,"class":6},"Copernicus Memorial Hospital","OTHER",[8,15,21],{"label":9,"type":10,"description":11,"interventionNames":12},"Transpedicular spinal stabilization using carbon system + SBRT","EXPERIMENTAL","Transpedicular spinal stabilization using a radiolucent composite system made of carbon fibers and PEEK followed by stereotactic radiotherapy of the spine at a dose of 5x5 Gy (25 Gy in the total dose)",[13,14],"Procedure: Transpedicular spinal stabilization - carbon fibers-based implants","Radiation: Stereotactic body radiotherapy",{"label":16,"type":17,"description":18,"interventionNames":19},"Transpedicular spinal stabilization using titanium system + SBRT","ACTIVE_COMPARATOR","Transpedicular spinal stabilization using a titanium system followed by stereotactic radiotherapy of the spine at a dose of 5x5 Gy (25 Gy in the total dose)",[20,14],"Procedure: Transpedicular spinal stabilization - titanium implants",{"label":22,"type":23,"description":24,"interventionNames":25},"SBRT + Transpedicular spinal stabilization using titanium system","SHAM_COMPARATOR","Transpedicular spinal stabilization using a titanium system preceded with stereotactic spine radiotherapy at a dose of 5x5 Gy (25 Gy in the total dose) as the first stage of treatment",[20,14],[27,33,37],{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"PROCEDURE","Transpedicular spinal stabilization - carbon fibers-based implants","Transpedicular stabilization with carbon fiber and PEEK-based implants in one of the two possible variants - first involves a large skin incision and separation of the back extensor muscles; second is associated with minimally invasive, which is percutaneous procedure that allows the stabilization with implants without the need to detach the muscles, using only a small skin incision.",[9],null,{"type":28,"name":34,"description":35,"armGroupLabels":36,"otherNames":32},"Transpedicular spinal stabilization - titanium implants","Transpedicular stabilization with titanium implants in one of the two possible variants - first involves a large skin incision and separation of the back extensor muscles; second is associated with minimally invasive, which is percutaneous procedure that allows the stabilization with implants without the need to detach the muscles, using only a small skin incision.",[22,16],{"type":38,"name":39,"description":40,"armGroupLabels":41,"otherNames":42},"RADIATION","Stereotactic body radiotherapy","Spinal tumors will be treated with stereotactic body radiotherapy at a dose of 5x5 Gy (25 Gy in a total dose); either prior to or post-surgical treatment, accordingly the allocation to one of the study arms.",[22,9,16],[43],"SBRT",[45],{"name":46,"affiliation":47,"role":48},"Kamil Krystkiewicz, PhD","Department of Neurosurgery and Neurooncology, Copernicus Memoriał Hospital in Łódź","PRINCIPAL_INVESTIGATOR",[50,54],{"name":46,"role":51,"phone":52,"phoneExt":32,"email":53},"CONTACT","+48426895341","kamil.krystkiewicz@gmail.com",{"name":55,"role":51,"phone":52,"phoneExt":32,"email":56},"Marcin Tosik, PhD","sekretariat.neurochirurgia@kopernik.lodz.pl",[58,70,75,83,88],{"facility":59,"status":60,"city":61,"state":32,"zip":32,"country":62,"countryCode":63,"cosmosGeoPoint":64,"geoPoint":69,"contacts":32},"Department of Neurosurgery, Functional Neurosurgery and Stereotaxy, Dr. Jan Biziel University Hospital No. 2 in Bydgoszcz","ACTIVE_NOT_RECRUITING","Bydgoszcz","Poland","PL",{"type":65,"coordinates":66},"Point",[67,68],18.00762,53.1235,{"lat":68,"lon":67},{"facility":71,"status":60,"city":61,"state":32,"zip":32,"country":62,"countryCode":63,"cosmosGeoPoint":72,"geoPoint":74,"contacts":32},"Professor Franciszek Łukaszczyk Oncology Center in Bydgoszcz - National Research Institute",{"type":65,"coordinates":73},[67,68],{"lat":68,"lon":67},{"facility":76,"status":60,"city":77,"state":32,"zip":32,"country":62,"countryCode":63,"cosmosGeoPoint":78,"geoPoint":82,"contacts":32},"Department of Teleradiotherapy, Lower Silesian Center of Oncology, Pulmonology and Hematology","Wroclaw",{"type":65,"coordinates":79},[80,81],17.03006,51.10286,{"lat":81,"lon":80},{"facility":84,"status":60,"city":77,"state":32,"zip":32,"country":62,"countryCode":63,"cosmosGeoPoint":85,"geoPoint":87,"contacts":32},"University Center of Neurology and Neurosurgery, Jan Mikulicz-Radecki University Clinical Hospital in Wrocław",{"type":65,"coordinates":86},[80,81],{"lat":81,"lon":80},{"facility":89,"status":90,"city":91,"state":92,"zip":93,"country":62,"countryCode":63,"cosmosGeoPoint":94,"geoPoint":98,"contacts":99},"Copernicus Memorial Hospital in Łódź, Poland","RECRUITING","Lodz","Łódź Voivodeship","93-513",{"type":65,"coordinates":95},[96,97],19.47395,51.77058,{"lat":97,"lon":96},[100],{"name":46,"role":51,"phone":52,"phoneExt":32,"email":53},{"type":48,"investigatorFullName":102,"investigatorTitle":103,"investigatorAffiliation":5,"oldNameTitle":32,"oldOrganization":32},"Kamil Krystkiewicz","Principal Investigator",[105],{"name":106,"class":107},"Medical Research Agency, Poland","OTHER_GOV","100538616","carbon-fiber-transpedicular-screws-in-treatment-of-spinal-metastatic-disease-100538616",false,"NCT06293157","Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease","Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease and Stereotactic Radiotherapy - a Prospective, Randomized Trial","CarboMetaspine","Inclusion Criteria:\n\n* Metastatic spinal disease,\n* ECOG quality of life of 0-2,\n* Eligibility for SBRT treatment,\n* Expected survival time \\>3 months,\n* Signed informed consent to participate in the study,\n* Sufficient organ capacity allowing to survive the perioperative period.\n\nExclusion Criteria:\n\n* Primary tumor of the spine,\n* Age \\\u003C18 years old,\n* Expected survival time \\\u003C3 months,\n* Eligibility for palliative radiotherapy,\n* No informed consent to participate in the study,\n* Pregnancy or breastfeeding,\n* The advancement of the disease preventing the technical use of implants.","ALL","18 Years",{"count":119,"type":120},226,"ESTIMATED","INTERVENTIONAL",[123],"NA","Background: Spinal metastatic disease constitute a serious clinical problem in oncology. Bones are the third most common organ where metastases are located, and the spine is the place where they are most often located. Due to the complexity of the clinical problem, metastatic spine disease remains of interest to many medical specialties: neurosurgery, orthopedics, clinical oncology, radiotherapy and rehabilitation. With the development of modern diagnostic methods and wider access to them, the demand for neurosurgical treatment in this group of patients is growing. Surgical treatment is undertaken in cases of spinal cord compression, instability, spinal deformation or pain that is resistant to radiotherapy. The standard treatment in most cases is posterior instrumentation of the spine using titanium pedicle screws. Unfortunately, these systems cause numerous artifacts in diagnostic imaging, both in CT and MRI. These distortions make it difficult to plan radiotherapy and determine the optimal dose that would avoid healthy tissues. Moreover, artifacts could make difficult postoperative follow-ups aimed at assessing local recurrence. The solution to these problems is the use of radiolucent implants. There are systems based on carbon fibers embedded in PEEK which do not cause typical artifacts for titanium implants.\n\nStudy plan: The open, three-arm, prospective randomized study is planned to involve 226 patients with metastatic disease of the spine, with a known or undiagnosed primary site. Patients will be qualified for 2 types of interventions. The first one includes treatment with stereotactic radiotherapy (SBRT) in the first stage of treatment and early instrumentation of the spine with titanium implants. The second type of intervention includes patients qualified for surgical treatment using spine stabilization and postoperative SBRT. Patients within this arm will be randomized into two groups differing in the type of material the instrumentation is made of: carbon-PEEK or titanium. The study group will be patients stabilized with carbon implants, and the control group will be those who will have titanium implants.\n\nStudy population: The study includes adult patients with metastatic spine disease, with a known or unknown primary tumor, qualified for SBRT and surgical treatment.\n\nAssumed effects: It is assumed that the treatment proposed in the project would extend progression free survival by several months or achieve local control in an additional 5% of patients. Moreover, by improving the quality of imaging, earlier diagnosis of local recurrences and implementation of appropriate locoregional treatment would be possible.",[126,127],"Metastatic Spinal Cord Compression","Metastasis Spine",[129,130,131,132],"metastatic spinal disease","stereotactic body radiotherapy","spinal cord compression","carbon fiber reinforced implants","2025-12-08",{"date":135,"type":136},"2025-12-16","ACTUAL",{"date":138,"type":136},"2023-12-01",{"date":140,"type":120},"2033-12-31",{"name":5,"class":6},5]