[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"clinical-performance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:clinical-performance":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100642858","clinical-performance-and-multitasking-in-anesthesia--a-simulation-based-study-100642858",false,"NCT07615582","Clinical Performance and Multitasking in Anesthesia : a Simulation-based Study","FOCUS","Inclusion Criteria:\n\n* Anesthesiology and intensive care resident or attending physician\n* Written informed consent\n\nExclusion Criteria:\n\n* None",true,"ALL","18 Years",{"count":20,"type":21},35,"ESTIMATED","OBSERVATIONAL","Cognitive failure under multitasking conditions has been demonstrated in various settings, including healthcare. However, in anesthesiology, the impact of multitasking on clinical performance has not yet been fully characterized.\n\nThe objective of our study is to evaluate the impact of multitasking on anesthesiologists' clinical performance in a simulated setting.",[25,26,27,28,29,30],"Multitasking Behavior and Multitasking Ability","Clinical Performance","Simulation Training","Simulation Based Medical Education","Clinical Reasoning","Anesthesia","RECRUITING","2026-06-30",{"date":34,"type":35},"2026-07-02","ACTUAL",{"date":37,"type":35},"2026-06-09",{"date":39,"type":21},"2026-12",{"name":41,"class":42},"University Hospital, Grenoble","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":17,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100643976","effect-of-different-cavity-designs-on-the-clinical-performance-of-3d--printed-resin-composite-partial-coverage-restorations-in-vital-molars-100643976","NCT07667946","Effect of Different Cavity Designs on the Clinical Performance of 3D- Printed Resin Composite Partial-Coverage Restorations in Vital Molars","Effect of Different Cavity Designs on the Clinical Performance of 3D- Printed Resin Composite Partial-Coverage Restorations in Vital Molars With Complex Cavities: An 18 Month Randomized Clinical Trial","Inclusion Criteria:\n\n1. Adult patients aging 20-45 years.\n2. Healthy males and females\n3. Patients with good oral hygiene\n4. Patients presenting with at least one eligible permanent molar requiring a partial-coverage restoration.\n5. Patients willing and able to attend scheduled follow-up visits for 18 months.\n6. Permanent maxillary or mandibular molars.\n7. Vital teeth with a positive response to cold thermal testing.\n8. Complex Large or severely compromised cavities resulting from primary or secondary caries (ICDAS 5 or 6) and\u002For replacement of large defective restorations with at least 2 missing cavity walls requiring overlay restorations\n9. Well-formed and fully erupted in normal functional occlusion with natural antagonist and adjacent teeth.\n10. Absence of any radiographic, periodontal or periapical changes.\n\nExclusion Criteria:\n\n1. Participants with general\u002Fsystemic illness.\n2. Pregnant or lactating females.\n3. Concomitant participation in another research study.\n4. Inability or unwillingness to comply with study visits and procedures.\n5. Heavy bruxism or other parafunctional habits\n6. Known allergic reactions against any components of the used materials\n7. Patients receiving orthodontic treatment.\n8. Poor oral hygiene or high caries activity.\n9. Non vital teeth.\n10. Hypersensitive teeth.\n11. Teeth with prior endodontic treatment.\n12. Teeth with spontaneous pain or signs\u002Fsymptoms of irreversible pulpitis.\n13. Teeth with advanced periodontal disease or mobility.\n14. Teeth with a history of direct or indirect pulp capping procedure.\n15. Teeth with vertical root fractures or cracked tooth syndrome","20 Years","45 Years",{"count":54,"type":21},50,"INTERVENTIONAL",[57],"NA","This randomized clinical trial aims to evaluate the effect of different cavity designs on the clinical performance of 3D-printed resin composite partial-coverage restorations in vital molars with complex cavities over an 18-month follow-up period.",[26],"NOT_YET_RECRUITING","2026-06-19",{"date":63,"type":35},"2026-06-25",{"date":65,"type":21},"2026-07",{"date":67,"type":21},"2028-01",{"name":69,"class":42},"Cairo University"]