[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cervical-caries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cervical-caries":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,39,67,91,116],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":4},"100638961","clinical-evaluation-of-self-adhesive-flowable-giomer-with-and-without-selective-enamel-etching-100638961",false,"NCT07575646","Clinical Evaluation of Self-Adhesive Flowable Giomer With and Without Selective Enamel Etching","18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer With and Without Selective Enamel Etching Versus Flowable Giomer Using Standard Bonding Protocol in Carious Cervical Lesions: A Randomized Clinical Trial","Inclusion Criteria:\n\n1. Cervical carious lesions in anterior teeth and premolars\n2. Small to moderate class V carious lesion (ICDAS 3 \\& 4).\n3. Vital upper or lower periodontally sound teeth with no signs of irreversible pulpitis.\n4. Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth\n\nExclusion Criteria:\n\n1. Cervical carious lesions in molars.\n2. Deep carious defects (close to pulp, less than 1 mm distance).\n3. Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.\n4. Non-vital teeth, Fractured or cracked teeth.\n5. Endodontically treated teeth.\n6. Periodontally affected teeth","ALL","18 Years",{"count":19,"type":20},75,"ESTIMATED","INTERVENTIONAL",[23],"NA","This randomized clinical trial is to evaluate the clinical performance of the self-adhesive flowable Giomer with and without selective enamel etching compared to flowable Giomer using standard bonding protocol in class V cavity restorations over a period of 18 months.",[26],"Cervical Caries","NOT_YET_RECRUITING","2026-05-04",{"date":30,"type":31},"2026-05-08","ACTUAL",{"date":33,"type":20},"2026-07",{"date":35,"type":20},"2028-01",{"name":37,"class":38},"Cairo University","OTHER",{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":44,"targetDuration":4,"studyType":21,"phases":46,"briefSummary":47,"conditions":48,"keywords":49,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":4},"100588802","18-month-clinical-evaluation-of-self-adhesive-flowable-giomer-compared-to-conventional-flowable-giomer-in-carious-cervical-lesions-a-randomized-clinical-trial-100588802","NCT06946134","18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer Compared to Conventional Flowable Giomer in Carious Cervical Lesions: A Randomized Clinical Trial",{"count":45,"type":20},34,[23],"The material under investigation will offer the patient a high strength and high durability restoration with the advantage of having anti-bacterial properties.",[26],[50,51,52,53,54,55,56,57,58],"Self-adhesive giomer","Bioactive","Randomized clinical trial.","USPHS criteria","Carious cervical lesion","Class V","Clinical performance","FIT SA","Beautifil Flow Plus","2025-04-19",{"date":61,"type":31},"2025-04-27",{"date":63,"type":20},"2025-09",{"date":65,"type":20},"2027-02",{"name":37,"class":38},{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":74,"enrollmentInfo":75,"targetDuration":4,"studyType":21,"phases":76,"briefSummary":77,"conditions":78,"keywords":80,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":4},"100585368","the-effectiveness-rmgi-and-giomer-individually-and-combined-anterior-cervical-caries-100585368","NCT06901453","The Effectiveness RMGI and Giomer, Individually and Combined Anterior Cervical Caries","Effectiveness of RMGI and Giomer, Both Individually and in Combination, for Restoring Anterior Cervical Caries in High-Risk Patients: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Patient age range from 18-55 years\n* Presence of anterior cervical caries on the labial surface (ICDAS 4 \\& 5)\n* High caries risk\n* Good general health\n\nExclusion Criteria:\n\n* Severe or chronic periodontal disease\n* Bruxism\n* Non-vital teeth\n* Fractured or cracked teeth\n* Defective restorations\n* Pregnancy and\u002For lactation\n* Allergy to the main components of the products to be used in the study","55 Years",{"count":19,"type":20},[23],"This study compares the effectiveness of three dental materials for restoring anterior cervical caries in high-risk patients: resin-modified glass ionomer (RMGI), Giomer, and a combination technique where RMGI is veneered with Giomer. The 18-month randomized clinical trial will assess 75 patients (25 per group), primarily evaluating secondary caries formation, with additional measurements of restoration integrity, appearance, and sensitivity at baseline, 6, 12, and 18 months.",[79,26],"Dental Caries",[81,82],"Risk Factor","Patient Outcome Assessment","2025-03-23",{"date":85,"type":31},"2025-03-30",{"date":87,"type":20},"2025-05-01",{"date":89,"type":20},"2027-05-01",{"name":37,"class":38},{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":98,"sex":16,"minAge":99,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":115},"100560052","clinical-performance-of-ars-containing-universal-adhesives-in-carious-cervical-lesions-100560052","NCT06572124","Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions","Clinical Performance of Universal Adhesive with and Without Acid Resistant Silane Coupling Agent in Carious Cervical Lesions :A Randomized Controlled Trial","Inclusion Criteria:\n\n* Participants Inclusion:\n\n  • Adults aging from 21-67 years old who were in need of restoration of at least one notch-shaped cervical lesion\n* Teeth Inclusion:\n\n  * Vital teeth with carious cervical lesions in incisors , canines ,premolars\\& molars\n\nExclusion Criteria:\n\n* Participants Exclusion:\n\n  * Patients with fewer than 20 teeth\n  * Poor oral hygiene\n  * Uncontrolled periodontal disease\n  * Xerostomia\n  * Known allergy to resin-based materials\n  * Medically compromised, pregnant, or breast-feeding\n* Teeth Exclusion:\n\n  * Non vital teeth\n  * Teeth that are out of occlusion\n  * Previously restored teeth",true,"21 Years","67 Years",{"count":102,"type":20},80,[23],"Evaluation of composite restorations done in carious cervical lesions restored by a conventional universal adhesive in comparison to a universal adhesive that contains and resistant silane coupling agent according to the Modified United States Public Health Service (USPHS) criteria over 18 months.",[106,26],"Carious Lesion","2024-08-30",{"date":109,"type":31},"2024-09-04",{"date":111,"type":20},"2024-09-01",{"date":113,"type":20},"2026-04-30",{"name":37,"class":38},1,{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":98,"sex":16,"minAge":17,"maxAge":123,"enrollmentInfo":124,"targetDuration":4,"studyType":21,"phases":126,"briefSummary":127,"conditions":128,"keywords":4,"overallStatus":129,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":115},"100546400","clinical-evaluation-of-self-adhesive-bulk-fill-composite-versus-conventional-nano-hybrid-composite-in-cervical-cavities-100546400","NCT06394440","Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities","Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities - A Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Cervical lesions.\n* Cervical lesions of at least one mm depth; to include enamel and dentin.\n* Cervical lesions of not more than 3 mm in depth.\n* Male or female genders.\n* Medically free patients.\n* Normal occlusion.\n* Healthy Gingiva\n\nExclusion Criteria:\n\n* Teeth showing signs of pulpitis or periapical pathosis.\n* Patients older than 60 years.\n* Patients younger than 18 years old.\n* Pregnant women.\n* Patients with history of allergy to resin.\n* Patients with disabilities.\n* Carious cervical lesions extending to proximal surfaces.\n* Carious cervical lesions on the palatal\u002Flingual surfaces.\n* Teeth with root caries.\n* Endodontically treated teeth.","60 Years",{"count":125,"type":20},54,[23],"The aim of this randomized clinical trial is to compare the six months clinical performance of the self-adhesive bulk-fill composite with the conventional nano-hybrid composite in the cervical lesions of teeth in the esthetic zone. In addition, to evaluate patient's satisfaction towards the self-adhesive bulk-fill material and its total operatory time.",[26],"RECRUITING","2024-07-04",{"date":132,"type":31},"2024-07-08",{"date":134,"type":31},"2023-03-14",{"date":136,"type":20},"2024-07-30",{"name":138,"class":38},"Misr International University"]