[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dental-restorations\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dental-restorations":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,63,101],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":50,"whyStopped":4,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":62},"100589516","clinical-investigation-measuring-the-long-term-clinical-performance-and-safety-of-biodentine-xp-in-patients-treated-for-coronal-restorative-or-endodontic-dental-indications-100589516",false,"NCT06955429","Clinical Investigation Measuring the Long Term Clinical Performance and Safety of Biodentine™ XP in Patients Treated for Coronal Restorative or Endodontic Dental Indications.","Observational, Prospective, International and Multicenter Clinical Investigation Measuring the Longterm Clinical Performance and Safety of Biodentine™ XP in Patients Treated for Coronal Restorative or Endodontic Dental Indications.","BIOD XP","Inclusion Criteria:\n\n1. Temporary tooth, from a child ≥ 2 years old, requiring dental restorative treatment with Biodentine™ XP, and\u002For, Permanent (mature or immature) tooth, from a child or an adult, requiring a dental restorative and\u002For an endodontic treatment with Biodentine™ XP.\n2. Adult patient with a signed informed consent form; For the minor, if in age to understand, an assent is required, and at least one parent or legal representative must consent.\n3. Only in France: Subject affiliated or benefiting from a social\u002Fhealth insurance system.\n\nExclusion Criteria:\n\n1. Patient with one or more documented contraindication to use Biodentine™ XP (Refer to IFU).\n2. Inadequate expected tooth lifetime as estimated by the investigator:\n\n   * For a Temporary tooth: high probability of tooth loss within 2 years after treatment with Biodentine™ XP.\n   * For a permanent tooth: high probability of tooth loss within 10 years after treatment with Biodentine™ XP.\n3. Patient with any systemic disease that may hinder the normal healing process and\u002For the follow-up.\n4. Adult patient under legal protection measures or unable to express his\u002Fher consent, and individual deprived of liberty by judicial or administrative decision, as well as individual receiving psychiatric care.\n5. Periodontitis (stage 3, 4 or stage 2 grade C).\n6. Inability to comply with study procedures.\n7. Participation in another interventional clinical investigation that can induce bias in the study results.","ALL","2 Years",{"count":20,"type":21},275,"ESTIMATED","OBSERVATIONAL","The aim of this present study is to collect additional data for the post-marketing follow-up of Biodentine™ XP and measure long-term (up to 10 years) performance and safety of the biomaterial in all its indications.",[25,26,27],"Dental Restoration, Permanent","Dental Restorations","Endodontic Treatment",[29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49],"Dentine restoration","Coronal carious lesions","Restoration of cervical lesion","Restoration of radicular lesion","Pulp capping","Pulpotomy","Apexification","Revitalization","Endodontic treatment","Root","Crown","Pulp","Root perforations","Furcation perforations","Perforating internal resorptions","External resorption","Root-end filling","Permanent dentine restoration","Temporary dentine-enamel restoration","Biodentine","Biodentine XP","RECRUITING","2026-04-30",{"date":53,"type":54},"2026-05-06","ACTUAL",{"date":56,"type":54},"2025-10-23",{"date":58,"type":21},"2037-02-28",{"name":60,"class":61},"Septodont","INDUSTRY",8,{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":71,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":72,"targetDuration":4,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":83,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":4},"100582368","sequential-practicing-on-psychomotor-skill-acquisition-in-undergraduate-dental-students-100582368","NCT06862401","Sequential Practicing on Psychomotor Skill Acquisition in Undergraduate Dental Students","Influence of Sequential Practicing for Psychomotor Skill Acquisition of Non-dominant Hand in Undergraduate Dental Students: A Randomized Controlled Trial With Qualitative Approach","Dentalpractice","Inclusion Criteria:\n\n1. The fourth- to sixth-year undergraduate dental students at a single setting of school\n2. The fifth- and sixth-year students had completed laboratory and lecture courses in operative and fixed dental prosthodontics\n3. The fourth-year students are enrolled in their final laboratory and lecture courses in fixed prosthodontics.\n\nExclusion Criteria:\n\nUndergraduate dental students who have prior experience with onlay preparation in laboratory or clinical settings or those who are unwillingness to adhere to the study protocol.",true,{"count":73,"type":21},28,"INTERVENTIONAL",[76],"NA","To determine the influence of hand practice sequence on psychomotor skill acquisition in a glass ceramic onlay preparation among undergraduate dental students.",[79,26,80,81,82],"Undergraduate Health Professional Students","Education, Competency-Based","Dental Education and Special Care Dentistry","Dental Prosthesis",[84,85,86,87,88,89],"dominant hand","sequential practice","healthcare","dental education","prosthodontic","competency","NOT_YET_RECRUITING","2025-03-27",{"date":93,"type":54},"2025-04-02",{"date":95,"type":21},"2025-03-31",{"date":97,"type":21},"2025-07-04",{"name":99,"class":100},"Chulalongkorn University","OTHER",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":4,"eligibilityCriteria":107,"healthyVolunteers":11,"sex":17,"minAge":108,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":111,"conditions":112,"keywords":4,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":4},"100567851","a-clinical-study-collecting-patients-experience-during-dental-implant-treatment-100567851","NCT06673563","A Clinical Study Collecting Patients' Experience During Dental Implant Treatment","Development and Evaluation of a Patient-reported Experience Measure (PREM) in Implant Dentistry: an Exploratory Study","Inclusion Criteria:\n\n* Subject signed informed consent\n* Subject is at least 18 years old at the time of treatment\n* Subject presented with the need of dental implant treatment for single tooth, multiple teeth, or full-arch rehabilitation\n* Subject with medical and anatomical conditions that are in accordance with the applicable instructions for use (IFU)\n* Subject agree to provide information on her\u002Fhis experience and outcomes before, during and after the treatment\n* Subject has a working e-mail address\n* Subject has sufficient English language skills for answering the PREM questionnaires\n\nExclusion Criteria:\n\n* Anatomical conditions discovered during surgery preventing the use of intended implant system\n* Subject with history of allergy or adverse reactions to any materials used\n* Uncontrolled unstable systemic disease\n* Any ongoing application of medication that is interfering with the dental treatment\n* Subject is not willing \u002F unable to complete the PREM questionnaires\n* Subject that is planning not to return to the investigational site for follow-up visits within study schedule\n* Pregnant or lactating women at the time of implant insertion","18 Years",{"count":110,"type":21},99,"The study will gather data on patient reported experience (PREM) before, during and after dental implant treatment. Patients scheduled in three treatment groups for either single tooth, multiple teeth or full-arch dental rehabilitation are included in the study and will be treated according standard of care. Additionally, they are asked to report their experience based on pre-defined questionnaire assessing patient acceptance of implant treatment in dentistry. Patients will be followed-up until 1-Year post Final Prosthesis Delivery.\n\nThis studies primary endpoint is the completion of the PREM questionnaires. The study is not intended to investigate safety and performance of the used medical devices.",[113,26,114,115],"Dental Implant","Patient Reported Outcome","Patient Experience","2024-11-02",{"date":118,"type":54},"2024-11-05",{"date":120,"type":21},"2025-01",{"date":122,"type":21},"2026-10",{"name":124,"class":100},"Dr Robert Bowe"]