[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"robotic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:robotic":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,56],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":36,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":4},"100653295","surgweek-2-identifying-the-global-burden-of-post-operative-complications-an-international-prospective-cohort-study-protocol-100653295",false,"NCT07785076","SurgWeek-2: Identifying the Global Burden of Post Operative Complications: an International Prospective Cohort Study Protocol","SurgWeek-2","Inclusion Criteria:\n\n* Any operation (elective or emergency) performed in an operating theatre is eligible for inclusion, except for minor procedures specified in Appendix A.\n* All surgical specialties can participate including acute care surgery, breast surgery, cardiac surgery, colorectal surgery, general surgery, gynaecology, hepatobiliary surgery, neurosurgery, obstetrics, oesophagogastric surgery, ophthalmology, oral and maxillofacial surgery, orthopaedics, otolaryngology, paediatric surgery, plastic surgery, thoracic surgery, transplant surgery, trauma surgery, urology and vascular surgery.\n* Patients undergoing both day case surgery and inpatient surgery should be included.\n\nExclusion Criteria:\n\n* Patients who do not undergo an operation (e.g. planned operations that are cancelled).\n* Patients undergoing angiography or minor procedures.\n* Procedures performed outside of an operating theatre\n* Individual participating centres can choose to include children only, adults only, or both children and adults. If including children or adults only, an age cut off should be selected that is appropriate to the local context.\n* Each individual patient should only be included in the study once, based on the first operation they undergo within the data capture window. Therefore, patients who are re-operated within 30-days should only be entered once.",true,"ALL",{"count":19,"type":20},100000,"ESTIMATED","30 Days","OBSERVATIONAL","This study aims to assess and improve the global outcomes following surgery. Every year approximately 313 million operations are performed, with 50 million people experiencing a complication and unfortunately 3.5 million people will die following these operations. This study will assess how outcomes vary following surgery throughout the world and explore system access, quality and efficiency.\n\nThe secondary aims of this study are to (1) assess the use of antibiotics and the impact of resistant organisms globally, (2) assess who dies after an operation and whether there are factors that were identified that could have prevented the death, (3) assess the assess and outcomes to minimally invasive and robotic surgery, (4) assess the outcomes of the Bellwether procedures (laparotomy, caesarean delivery, open fracture management) as these are conditions used to assess the functioning of a health system.\n\nThe study will take place for six week in May-June 2026 and will aim to collect data from 100,000 patients across 1000 hospitals in 100 countries to give a global perspective on the above outcome measures. The data will be analysed by hospital income group to understand how resources impact on outcomes.\n\nBy combining global data on clinical outcomes with information on hospital resources, this study hopes to provide valuable insights into how to improve surgical care across diverse settings, making recommendations that lead to better access to safe, timely and affordable care for surgical problems worldwide.",[25,26,27,28,29,30,31,32,33,34,35],"Surgery Complications","Surgery","Global Surgery","Robotic","Laparotomy","Caesarean Section","Open Fracture","Antimicrobial","Mortality","Bellwether","Minimally Invasive Surgery",[37,38,29,39,40,41,42,43],"Complications","mortality","Caesarean Delivery\u002FSection","Open fracture","Antimicrobial use","Robotic surgery","Minimally invasive surgery","NOT_YET_RECRUITING","2026-08-20",{"date":47,"type":48},"2026-08-25","ACTUAL",{"date":50,"type":20},"2026-08-31",{"date":52,"type":20},"2027-03",{"name":54,"class":55},"University of Birmingham","OTHER",{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":11,"sex":17,"minAge":63,"maxAge":4,"enrollmentInfo":64,"targetDuration":4,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":72,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":89},"100482678","flapless-zygomatic-implants-robot-assisted-placement-100482678","NCT05565157","Flapless Zygomatic Implants Robot-assisted Placement","ROSA-ZYGOMA","Inclusion Criteria:\n\n* Patients suffering from Maxillary edentulism with severe bone resorption\n* Patients suffering from maxillary edentulism post maxillary defect (carcinologic or traumatic) and free flap reconstruction\n* Patients suffering from post-maxillectomy buccosinusal communication.\n* Age ≥ 18 years old\n* Having signed the informed consent\n\nExclusion Criteria:\n\n* Patients suffering from chronic sinusitis\n* Patients refusing ROSA robot-guided surgery (unsigned informed consent).\n* Pregnant and nursing women","18 Years",{"count":65,"type":20},15,"INTERVENTIONAL",[68],"NA","Zygomatic implants are indicated for the rehabilitation of the severely atrophic maxilla. Similar to standard implant placement, gaining an optimal position of the zygomatic implants is essential for a predictable prosthetic-driven treatment outcome.\n\nHowever, there is no effective mechanism to physically control the drilling trajectory for the zygomatic implants. Therefore, deviation between the actual and planned implant position is inevitable.\n\nThis approach is technically difficult, and is performed by an experienced surgeon.\n\nThe development of a surgical technique that is both safer and less invasive is currently possible thanks to robotics. In this project, a robotic assisted new strategy for positioning zygomatic implants will be performed and its efficacy and accuracy will be assess.\n\nPath planning will be carried out on a pre-operative scanner. The ROSA robot (Zimmer®) will guide the several drillings steps. Placement of the zygomatic implant will be performed manually.",[71,28],"Zygomatic Implant",[73,74,75,76,77,78],"zygomatic implant","robotic","flapless","mini-invasive","ROSA","immediate loading","RECRUITING","2024-07-09",{"date":82,"type":48},"2024-07-10",{"date":84,"type":48},"2022-09-30",{"date":86,"type":20},"2024-12",{"name":88,"class":55},"Centre Hospitalier Universitaire, Amiens",1]