[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626291":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":39,"locations":45,"responsibleParty":59,"collaborators":43,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":65,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":43,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":47,"whyStopped":43,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Baskent University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"3D-Printed Occlusal Splint (Voco V-Print)","EXPERIMENTAL","Participants will receive a custom-made occlusal splint fabricated by 3D printing using a photopolymer resin (Voco V-Print) following a standardized clinical workflow. The splint will be delivered and adjusted as needed and worn during sleep for 3 months.",[13,14],"Device: 3D-Printed Occlusal Splint (Voco V-Print)","Device: Conventional Acrylic Occlusal Splint",{"label":16,"type":17,"description":18,"interventionNames":19},"Conventional Acrylic Occlusal Splint","ACTIVE_COMPARATOR","Participants will receive a custom-made conventional occlusal splint fabricated from acrylic resin using standard laboratory techniques. The splint will be delivered and adjusted as needed and worn during sleep for 3 months.",[13,14],[21,29],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DEVICE","Custom-made occlusal splint manufactured by 3D printing using a photopolymer resin (Voco V-Print) and delivered with standardized instructions for use and care. Worn during sleep for 3 months.",[9,16],[26,27,28],"Occlusal Splint","Stabilization Splint","Michigan Splint",{"type":22,"name":16,"description":30,"armGroupLabels":31,"otherNames":32},"Custom-made conventional acrylic occlusal splint fabricated using standard techniques and delivered with standardized instructions for use and care. Worn during sleep for 3 months.",[9,16],[33,28],"Stabilization splint",[35],{"name":36,"affiliation":37,"role":38},"Hale Arıkan Kalaycı, Assistant Professor","Başkent University, Faculty of Dentistry","STUDY_DIRECTOR",[40],{"name":36,"role":41,"phone":42,"phoneExt":43,"email":44},"CONTACT","+903122466666",null,"halearikan@baskent.edu.tr",[46],{"facility":37,"status":47,"city":48,"state":43,"zip":49,"country":50,"countryCode":43,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"RECRUITING","Ankara","06490","Turkey (Türkiye)",{"type":52,"coordinates":53},"Point",[54,55],32.85427,39.91987,{"lat":55,"lon":54},[58],{"name":36,"role":41,"phone":42,"phoneExt":43,"email":44},{"type":60,"investigatorFullName":61,"investigatorTitle":62,"investigatorAffiliation":5,"oldNameTitle":43,"oldOrganization":43},"PRINCIPAL_INVESTIGATOR","Hale Arıkan Kalaycı","Assistant Professor","100626291","3d-printed-vs-conventional-acrylic-stabilization-splints-in-young-adults-with-bruxism-and-temporomandibular-disorders-a-randomized-trial-100626291",false,"NCT07433725","3D-Printed vs Conventional Acrylic Stabilization Splints in Young Adults With Bruxism and Temporomandibular Disorders: A Randomized Trial","Clinical Performance of Stabilization Splints Produced With a 3D Printer in the Treatment of Bruxism and Temporomandibular Disorders","3D PRINTED","Inclusion Criteria:\n\n* Adults (≥18 years) diagnosed with bruxism (sleep and\u002For awake bruxism) based on clinical assessment and patient report.\n\nIndication for an occlusal splint and willingness to wear the splint during sleep for 3 months.\n\nAbility to provide written informed consent and to attend scheduled follow-up visits.\n\nExclusion Criteria:\n\n* Current or recent use of an occlusal splint within the last 6 months.\n\nOngoing orthodontic treatment or planned major dental treatment during the study period that could affect occlusion.\n\nSevere temporomandibular disorder requiring active treatment (e.g., acute pain, limited mouth opening) or other conditions that could contraindicate splint use.\n\nExtensive untreated dental disease requiring immediate care (e.g., severe periodontal disease, multiple untreated caries).\n\nSystemic\u002Fneurologic conditions or medications that may significantly affect bruxism or neuromuscular function (as judged by the investigator).","ALL","18 Years","25 Years",{"count":75,"type":76},44,"ESTIMATED","INTERVENTIONAL",[79],"NA","This randomized clinical study will compare two occlusal splint (night guard) fabrication methods in adults with bruxism (teeth grinding\u002Fclenching). Forty-four participants will be randomly allocated to receive either (1) a 3D-printed splint manufactured from a photopolymer resin (Voco V-Print) or (2) a conventional acrylic splint fabricated using standard techniques. Participants will wear the splint during sleep for 3 months and will follow standardized instructions for use and care. At the 3-month follow-up, patient-reported satisfaction and oral health-related quality of life will be assessed using an OHIP-derived questionnaire, and splint wear will be quantified as volumetric material loss (mm³) by 3D scanning and superimposition. The results will help determine whether 3D-printed splints provide comparable patient-centered outcomes and clinical durability to conventional acrylic splints.",[82],"Bruxism, Sleep",[84],"occlusal splint","2026-02-19",{"date":87,"type":88},"2026-02-25","ACTUAL",{"date":90,"type":88},"2026-01-12",{"date":92,"type":76},"2026-08",{"name":5,"class":6},1]