[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"peri-implant-tissues\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:peri-implant-tissues":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,75],{"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":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100651468","comparison-between-socket-shield-and-conventional-techniques-in-immediate-implant-placement-100651468",false,"NCT07761442","Comparison Between Socket Shield and Conventional Techniques in Immediate Implant Placement.","Comparative Study Between Using Socket Shield And Conventional Techniques In Immediate Implant Placement (A Randomized Clinical Trial)","Inclusion Criteria:\n\n* Patients aged between 20 and 60 years of both genders\n* All participants should be systemically healthy, as assessed using the dental modification of the Cornell Medical Index.\n* Gingival and periodontal health to be confirmed according to the criteria outlined in the new classification system proposed by Caton et al. (2018).\n* Presence of non-restorable teeth due to trauma, complicated crowns or root fractures.\n* Presence of extensive destructive caries making the tooth unsalvageable, particularly in esthetic zones.\n* Clinical indication for immediate implant placement, especially in cases where minimizing post-extraction bone resorption and soft tissue collapse is critical.\n* Availability of adequate interocclusal space to accommodate the necessary prosthetic components without occlusal interference.\n\nExclusion Criteria:\n\n(for socket-shield technique)\n\n* Pregnant female.\n* Patients with parafunctional habits (e.g., bruxism, clenching).\n* Smokers.\n* Teeth with clinical mobility.\n* Teeth with root fractures extending below the alveolar bone level.\n* Periodontal ligament space widening.\n* Signs of internal or external root resorption.\n* Current or previous periodontal disease","ALL","20 Years","60 Years",{"count":20,"type":21},16,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this randomized clinical trial is to compare whether immediate implant placement using the socket-shield technique can better preserve bone density, bone level, and peri-implant tissue health compared to conventional immediate implant placement in patients requiring tooth extraction in the maxillary esthetic zone.\n\nThis study is conducted in systemically healthy adult patients aged 20-60 years who have non-restorable maxillary anterior teeth indicated for immediate implant placement.\n\nThe main questions this study aims to answer are:\n\nDoes the socket-shield technique result in better peri-implant bone density and bone level preservation compared to the conventional immediate implant technique?\n\nDoes the socket-shield technique lead to improved clinical peri-implant parameters, including probing depth, bleeding on probing, keratinized tissue width, and soft tissue thickness?\n\nparticipants will be divided into two groups: (both groups will receive immediate implant placement of a tooth requiring extraction in the maxillary esthetic zone.) First group: will recieve immediate implant using conventional technique. second group: will recieve immediate implant using socket shield technique.\n\nParticipants will:\n\n* Undergo clinical and radiographic examinations, including cone beam computed tomography (CBCT).\n* Receive immediate implant placement using either the conventional technique or the socket-shield technique.\n* Be followed up clinically and radiographically for 9 months to assess bone and soft tissue healing.\n* Attend regular postoperative and follow-up visits for evaluation of implant stability and peri-implant tissue health.",[27,28,29,30,31,32,33],"Bone Density","Bone Level","Peri-Implant Tissues","Socket Shield Technique Implant Placement","Immediate Implant Placement","Root Submergence Technique","Single Tooth Lost","RECRUITING","2026-08-10",{"date":37,"type":38},"2026-08-12","ACTUAL",{"date":40,"type":38},"2025-10-20",{"date":42,"type":21},"2026-11",{"name":44,"class":45},"Minia University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":16,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":46},"100638282","volumetric-analysis-of-peri-implant-soft-tissue-changes-between-polyethereketonepeek-anatomic-healing-abutments-and-standard-healing-abutments-in-posterior-single-implant-restorations-100638282","NCT07624331","Volumetric Analysis of Peri-Implant Soft Tissue Changes Between Polyethereketone(PEEK) Anatomic Healing Abutments and Standard Healing Abutments in Posterior Single Implant Restorations","anatomic","Inclusion Criteria:\n\nlegally competent to provide written informed consent form prior to any study related procedures.\n\n* Subjects of either sex or aged 18 above\n* requires replacement of a single missing posterior tooth with adequate mesiodistal dimension (≥8 mm)\n* intact adjacent teeth on both sides with existing opposing tooth condition\n* good oral hygiene, plaque score \\\u003C25% bpe1\n* adequate keratinized mucosa width (kmw) minimum 6 mm at the edentulous site\n* adequate bone volume to accommodate the planned dental implant placement of 5.5 mm diameter and 10 mm in length as verifified by Cone Beam Computed Tomography (CBCT)\n* adequate interoccusal distance (crown height space) of at least 6mm measured from alveolar crest to the occlusal table.\n\nExclusion Criteria:\n\nLocalized or generalized periodontitis\n\n* Presence of active acute infection\n* History of malignancy, radiotherapy or chemotherapy\n* Bone metabolic diseases (e.g.: osteogenesis imperfecta, Paget's disease) or current use of medications affecting bone metabolism\n* Untreated bruxism or parafunctional habits Docusign Envelope ID: FFD7C6C1-66CB-4359-9662-63230F769528 22\n* Severe occlusal discrepancy\n* Any medical condition contraindicating implant placement or alter daily activities to a level consistent with ASA (American Society of Anesthesiologist) III classification (including cardiovascular, hepatic, renal, gastrointestinal, metabolic, neurologic, pulmonary, endocrine, autoimmune or psychiatric disorders)\n* Subjects in need of bone grafting at the site of intended implantation site.\n* Subjects that are pregnant",true,"18 Years",{"count":57,"type":21},38,[24],"This prospective randomized clinical trial will evaluate the clinical outcomes of the implant crown fabricated with standard scan body (control) and polyetheretherketone (PEEK) anatomic healing abutment (test).",[61,29,62],"Peri-Implant Health","Soft Tissue Augmentation at Dental Implants",[29,64,65],"volumetric analysis","soft tissue","2026-05-31",{"date":68,"type":38},"2026-06-03",{"date":70,"type":21},"2026-05-23",{"date":72,"type":21},"2028-10-01",{"name":74,"class":45},"DR NUR HAFIZAH KAMAR AFFENDI",{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":87,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":46},"100573985","the-effect-of-injectable-platelet-rich-fibrin-in-peri-implant-soft-tissue-100573985","NCT06753396","The Effect of Injectable Platelet-Rich Fibrin in Peri-implant Soft Tissue","Evaluation of the Effect of Injectable Platelet-Rich Fibrin on Peri-Implant Soft Tissue Phenotype","Inclusion Criteria:\n\n1. be over 18 years old\n2. The patient does not have any systemic disease\n3. Patients who do not smoke or who smoke less than 10 cigarettes\n4. Peri-implant keratinized mucosa width less than 2 mm\n5. Peri-implant mucosal thickness less than 2 mm\n\nExclusion Criteria:\n\n1. Being out of the defined age group\n2. Any systematic contraindication for periodontal surgery\n3. Patients who smoke more than 10 cigarettes per day\n4. Patients with adequate peri-implant keratinized mucosa width and mucosal thickness\n5. Pregnancy\n6. Patients taking medication that suppresses the immune system or impairs healing\n7. Patients taking medication that impairs the bleeding condition",{"count":83,"type":21},80,[24],"An inadequate amount of peri-implant soft tissue results in more plaque accumulation around the implants, peri-implant mucositis, marginal bone loss, mucosal recession, and\u002For attachment loss. In the literature, there are studies evaluating the application of injectable platelet-rich fibrin to the gingiva and oral mucosa around teeth, but injectable platelet-rich fibrin application around implants has not been encountered. This study aimed to evaluate the effect of subgingival and submucosal application of injectable platelet-rich fibrin on peri-implant soft tissue phenotype in patients with inadequate peri-implant soft tissue phenotype.The study will include 80 systemically healthy and non-smoking patients\u002Fimplants older than 18 years of age with insufficient peri-implant keratinized mucosa width and mucosal thickness who applied to Kütahya University of Health Sciences, Faculty of Dentistry, Department of Periodontology. There are two study groups according to peri-implant mucosa phenotype: Thin phenotype and thick phenotype. All patients will undergo the same procedure of injectable platelet-rich fibrin application",[29],[88,89,90,91],"Peri-implant soft tissue","Injectable platelet-rich fibrin","Platelet-rich fibrin","Phenotype","2025-09-04",{"date":94,"type":38},"2025-09-11",{"date":96,"type":38},"2022-12-15",{"date":98,"type":21},"2026-04-15",{"name":100,"class":45},"Kutahya Health Sciences University"]