[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"soft-tissue-augmentation-around-dental-implants\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:soft-tissue-augmentation-around-dental-implants":74},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100594437",false,"NCT07019428","Clinical Evaluation of a Modified Technique for Free Gingival Graft Stabilization Using Titanium Fixation Tacs Around Implants Versus Conventional Suturing Technique","Clinical Evaluation of a Modified Technique for Free Gingival Graft Stabilization Using Titanium Fixation Tacs Around Implants Versus Conventional Suturing Technique: A Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Systemically healthy individuals of age ≥ 18 to 40 years with absence of active periodontal disease.\n* Having inadequate width of keratinized gingiva (\\\u003C 2 mm).\n* No systemic disease according to Modified Cornell Medical Index health questionnaire\n* Non-smoker.\n* Full mouth plaque index (PI) and full-mouth bleeding on probing (BOP) score of ≤ 15%.\n* No malocclusion, crowding, fillings, missing or supernumerary mandibular anterior teeth.\n* No blood-borne conditions.\n\nExclusion Criteria:\n\n* Active orthodontic treatment.\n* Previous periodontal surgery.\n* Systemic disease.\n* Use of blood thinners.\n* Use of any drugs that might lead to gingival enlargement.\n* Mucogingival stress, bruxism.\n* Pregnancy or lactation.",true,"ALL","18 Years","40 Years",{"count":20,"type":21},26,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this randomized, controlled, parallel-grouped, clinical trial is to evaluate the width of keratinized gingiva after free gingival graft stabilized by titanium fixation tacs compared to traditional suturing.\n\nResearch question:\n\nIn patients with inadequate keratinized gingiva undergoing soft tissue augmentation by free gingival graft , will graft stabilization using Titanium fixation tacs affect the amount of keratinized tissue gain compared to graft stabilization using sutures ?",[27,28,29],"Free Gingival Graft","Soft Tissue Augmentation Around Dental Implants","Inadequate Keratinized Tissue Around Dental Implants",[31,32,33],"Free gingival graft","Titanium tacks","Keratinized tissue","RECRUITING","2025-06-12",{"date":37,"type":38},"2025-06-13","ACTUAL",{"date":40,"type":38},"2024-11-02",{"date":42,"type":21},"2026-02-01",{"name":44,"class":45},"Cairo University","OTHER",1,{"id":48,"slug":4,"hasResults":10,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":5},"100594368","NCT07018531","Vertical Soft Tissue Augmentation With Tent Pole Technique and Its Influence on Marginal Bone Loss Around Dental Implants","Vertical Soft Tissue Augmentation Using the Tent-Pole Technique With Adjunctive Therapies and Its Influence on Marginal Bone Loss Around Dental Implants: A Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Participants must be over 18 years of age. They should be legally capable of adhering to study protocols, which include maintaining proper oral hygiene, attending all scheduled follow-up visits, fully understanding the proposed surgical procedures, and signing the informed consent form.\n* single edentulous sites in the premolar and\u002For molar region of the mandible.\n* Vertical gingival thickness must be more than 1 mm and less than or equal to 2 mm.\n* A minimum of 2 mm of attached gingiva should be present on both the buccal and lingual sides of the implant sites.\n* Buccal bone thickness must be at least 1.5 mm.\n\nExclusion Criteria:\n\n* Presence of general contraindications for dental implants or surgical interventions.\n* Heavy smoking, defined as more than 10 cigarettes daily, including pipe, vape or cigar use.\n* Poor oral hygiene, characterized by probing depths greater than 4 mm in adjacent teeth, and a full mouth plaque score (FMPS) or full mouth bleeding score (FMBS) exceeding 25% after the pre-treatment phase.\n* Guided bone regeneration at the implant site.\n* History of conditions or diseases that compromise bone metabolism (e.g. Paget's disease, osteoporosis) or current use of medications that may affect bone metabolism (e.g. bisphosphonates).\n* History of cancer or prior radiotherapy or chemotherapy treatments for malignancy.\n* Uncontrolled diabetes.\n* Current pregnancy or breastfeeding status.\n* Allergies to any products involved in the study.",{"count":54,"type":21},112,[24],"This study aims to evaluate the effectiveness of the tent pole technique in vertical peri-implant soft tissue augmentation and to assess its impact on marginal bone loss. Additionally, the adjunctive use of platelet-rich fibrin and photobiomodulation will be explored to determine their influence on the clinical outcomes of this procedure.",[28],[59,60,61,62,63,64],"Dental Implants","Vertical Soft Tissue","Tent Pole Technique","Platelet-Rich Fibrin","Photobiomodulation","Marginal Bone Loss","NOT_YET_RECRUITING",{"date":67,"type":38},"2025-06-17",{"date":69,"type":21},"2025-07",{"date":71,"type":21},"2026-08",{"name":73,"class":45},"University of Santiago de Compostela",""]