[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"primary-molars\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:primary-molars":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100631723","clinical-performance-of-four-restorative-materials-in-primary-molars-100631723",false,"NCT07504393","Clinical Performance of Four Restorative Materials in Primary Molars","Clinical Evaluation of an Alkasite Restoration Material (Cention N) and Self-cure Composite (Stela; SDI) Compared to Conventional Composite and Resin-modified Glass Ionomer in Primary Molars: A Randomized Clinical Trial","Inclusion Criteria:\n\n1. Age 4-8 years old.\n2. Primary molars indicated for restorative treatment.\n3. No pulp involvement or history of dental pain.\n4. Cooperative children (Frankl: +ve or ++ve).\n\nExclusion Criteria:\n\n1. Pulp exposure after caries removal or clinical signs of irreversible pulpitis\u002Fnecrosis.\n2. Severe developmental enamel defects or insufficient enamel for bonding.","ALL","4 Years","8 Years",{"count":20,"type":21},92,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized clinical trial aims to compare the clinical and radiographic performance of four direct restorative materials used for restoring carious primary molars in children. Eligible children aged 4-8 years with posterior primary molars requiring direct restoration will be randomly allocated (1:1:1:1) to receive one of the following materials: an alkasite restorative material (Cention N), a self-cure bulk-fill resin composite (Stela; SDI), a conventional light-cured nanohybrid resin composite (Beautifil II), or a resin-modified glass ionomer cement (Riva Light Cure). Restorations will be evaluated using the Fédération Dentaire Internationale (FDI) World Dental Federation criteria. Postoperative sensitivity will be assessed at 48 hours using a 0-10 visual analogue scale (VAS). Clinical and radiographic follow-up assessments will be conducted at baseline and at scheduled recall visits",[27,28],"Dental Caries","Primary Molars",[30,31,32,33,34,35,36,37],"stela","Primary molars","Pediatric dentistry","Direct restoration","Cention N","Nanohybrid composite","Resin-modified glass ionomer","FDI criteria","NOT_YET_RECRUITING","2026-03-27",{"date":41,"type":42},"2026-03-31","ACTUAL",{"date":44,"type":21},"2026-04-01",{"date":46,"type":21},"2026-11",{"name":48,"class":49},"Al-Azhar University","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},"100630495","clinical-and-radiographic-outcomes-of-lesion-sterilization-and-tissue-repair-using-zinc-oxide-6-gingerol-mix-versus-triple-antibiotic-paste-in-non-vital-primary-molars-100630495","NCT07488416","Clinical and Radiographic Outcomes of Lesion Sterilization and Tissue Repair Using Zinc Oxide\u002F 6-gingerol Mix Versus Triple Antibiotic Paste in Non-vital Primary Molars","Comparative Evaluation of Clinical and Radiographic Outcomes of Lesion Sterilization and Tissue Repair Using Zinc Oxide\u002F 6-gingerol Mix Versus Triple Antibiotic Paste in Non-vital Primary Molars: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Age from 4 to 8 years.\n* Both sexes\n* Children must have at least two restorable non-vital primary molars\n* Periapical radiolucency.\n* Pain on mastication.\n* Pathological mobility.\n* Internal or external root resorption.\n* Furcation involvement should not extend to the developing tooth germ.\n\nExclusion Criteria:\n\n* Presence of systemic diseases.\n* Teeth with physiological mobility near exfoliation time.\n* Teeth with vital pulp.",{"count":58,"type":21},60,[24],"This study aims to evaluate and compare the clinical and radiographic outcomes of Lesion sterilization and tissue repair using zinc oxide\u002F 6-gingerol mix versus triple antibiotic paste in non-vital primary molars.",[62,63,64,65,66,67,68,69,28],"Clinical Outcomes","Radiographic Outcomes","Lesion Sterilization","Tissue Repair","Zinc Oxide","6-gingerol","Triple Antibiotic Paste","Non-vital","RECRUITING","2026-03-18",{"date":73,"type":42},"2026-03-23",{"date":75,"type":42},"2024-10-01",{"date":77,"type":21},"2026-05-01",{"name":48,"class":49},1]