[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"missing-teeth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:missing-teeth":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,44,74,101,123,148,173,193,226],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"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":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100613787","short-term-observation-on-the-clinical-application-effect-of-astra-tech-implant-ev-short-implants-for-maxillary-sinus-elevation-100613787",false,"NCT07271134","Short-term Observation on the Clinical Application Effect of Astra Tech Implant EV Short Implants for Maxillary Sinus Elevation","Inclusion Criteria:\n\n* Patients aged over 18 years old with at least one area of the posterior dental arch having insufficient alveolar bone height (3-6 mm)\n* Patients are in good health and have no major systemic diseases such as diabetes or cardiovascular diseases, and no maxillary sinus lesions\n* They are willing to undergo implant restoration treatment and can complete at least 3-year follow-up.\n\nExclusion Criteria:\n\n* horizontal bone deficiency alveolar ridges,bone defects caused by tumor resection\n* excessive tobacco use (more than 10 cigarettes per day)\n* severe liver and kidney diseases\n* history of radiotherapy and chemotherapy in the head and neck region\n* uncontrolled diabetes\n* active periodontal disease\n* oral mucosal diseases in the treatment area or poor oral hygiene,\n* PI \\> 70%",true,"ALL","18 Years","80 Years",{"count":20,"type":21},36,"ESTIMATED","INTERVENTIONAL",[24],"NA","Short-term comparison of clinical application effects of Astra OsseoSpeed EV short implants and conventional implants for maxillary sinus elevation",[27],"Missing Teeth",[29,30],"Short implant","Maxillary sinus floor elevation","NOT_YET_RECRUITING","2025-12-08",{"date":34,"type":35},"2025-12-16","ACTUAL",{"date":37,"type":21},"2025-12-10",{"date":39,"type":21},"2028-07-30",{"name":41,"class":42},"Linhu Wang","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":17,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":59,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":43},"100597090","the-effect-of-enamel-matrix-derivatives-on-gingival-tissue-thickness-100597090","NCT07053969","The Effect Of Enamel Matrix Derivatives On Gingival Tissue Thickness","The Effect Of Enamel Matrix Derivatives On Gingival Tissue Thickness. A Randomized Controlled Trial.","Inclusion Criteria:\n\n1. Ability of subject to understand and the willingness to sign a written informed consent document.\n2. Males and females; Age 18 to 89 years old\n3. Require second stage implant uncovering\n4. In either the maxillary or mandibular arch\n5. Has consistent transportation for all clinical and study visits\n\nExclusion Criteria:\n\n1. Pregnancy, or those planning to become pregnant\n2. Allergy or any medical issue using EMD\n3. Non-English speaking\n4. Patients on anticoagulants\n5. Patients who object to the use of animal products",{"count":52,"type":21},32,[24],"Scientists do research to answer important questions which might help change or improve the way we do things in the future.\n\nThe investigators know that using Enamel Matrix Derivatives results in thicker gum tissues around teeth. This study will test to see if using EMD around implants results in thicker gum tissues around implants.",[56,27,57,58],"Dental Implantation","Periodontitis, Adult","Mucositis",[60,61,62,63],"Enamel Matrix Derivatives","EMD","Keratinized mucosa width","Mucosal thickness","RECRUITING","2025-11-10",{"date":67,"type":35},"2025-11-12",{"date":69,"type":35},"2025-08-31",{"date":71,"type":21},"2027-09",{"name":73,"class":42},"The University of Texas Health Science Center at San Antonio",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":87,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":43},"100599106","assessment-of-hard-and-soft-tissue-changes-following-xcm-versus-fgg-simultaneous-with-delayed-dental-implant-placement-100599106","NCT07080177","Assessment of Hard and Soft Tissue Changes Following XCM Versus FGG Simultaneous With Delayed Dental Implant Placement","Assessment of Hard and Soft Tissue Changes Following Xenogeneic Collagen Membrane Versus Free Gingival Graft Simultaneous With Delayed Dental Implant Placement: Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n1. Adults above the age of 18 years.\n2. Presence of 2mm or less of keratinized tissue width\n3. Sufficient alveolar ridge width minimum of 6 mm\n4. Patients with good oral hygiene as evidenced by plaque index (PI)\\\u003C1 and showing cooperation or compliance with treatment.\n\nExclusion Criteria:\n\n1. Patients diagnosed with periodontal diseases (Caton et al., 2018).\n2. Acute active infection at implant sites\n3. Patients with medical conditions that would compromise the surgical procedures; uncontrolled diabetes mellitus, taking intravenous bisphosphonates for treatment of osteoporosis and radiotherapy\n4. Patients with parafunctional habits.\n5. Smokers (≥10 cigarettes per day),","55 Years",{"count":83,"type":21},24,[24],"Teeth loss are usually associated with alterations of extraction sockets result in obviously absorbed alveolar ridges and are often accompanied with soft tissue atrophy such as narrow keratinized tissue and a shallow vestibule.\n\nLack of peri-implant keratinized tissue is a potential risk to peri-implant diseases. Although the role of width of KM in maintaining peri-implant health is a controversial topic, the majority of high-level evidence has suggested that a minimum KM width (KMW) of 2 mm around the dental implants is critical to maintain peri-implant health and the long-term survival of dental implants.",[27],[88,89,90,91],"xenogeneic collagen membrane","free gingival graft","xenogeneic collagen matrices","simultaneous implant placement","2025-09-08",{"date":94,"type":35},"2025-09-12",{"date":96,"type":21},"2025-09-22",{"date":98,"type":21},"2026-12",{"name":100,"class":42},"Cairo University",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":105,"acronym":4,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":107,"targetDuration":109,"studyType":110,"phases":4,"briefSummary":111,"conditions":112,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":43},"100516656","post-market-clinical-foiiow-up-pmcf-medical-device-md-of-z-systems-monotype-zirconia-dental-product-z5m-dental-implants-registry-100516656","NCT06007365","Post Market Clinical FoIIow up (PMCF) Medical Device (MD) of Z-Systems Monotype Zirconia Dental Product: Z5m Dental Implants Registry","Inclusion Criteria:\n\n* Adult patient (≥ 18 years) was or will be implanted with up to 5 implants of the Z-Systems Z5m product group\n* Patient has signed Informed Consent.\n\nExclusion Criteria:\n\n• Inability to give consent",{"count":108,"type":21},70,"5 Years","OBSERVATIONAL","Commercially pure (CP) titanium is the gold standard to produce dental implants because it has a huge volume of scientific publications over a period of more than 50 years, it is cheap and simple to produce (i.e., making dental implants economically \"affordable\") and comes in numerous specitic designs of screws tor various indications. That is why more than 95% of the implant market 5 dominated by titanlum.\n\nHowever, there is an innovation trend to manufacture implants from more inert and biocompatible materials. Ceramic implants represent a valuable alternative for expanding the patient base of clinicians, especially in cases with challenging aesthetic demand. Furthermore, there has been a significant increase in the number of patients requesting metal-free dentistry or bio-holistic implant treatments.\n\nIn the past, ceramics were often branded as \"inferior\" quality due to its reputation as being brittle but the growing volume of scientific publications specifically an zirconia are demonstrating that lt is comparable in fracture-strength with titanium implants. There is a clear market niche for zirconia implants, especially in cases of:\n\n* Aesthetic reconstructions in the anterior region, especially in patients with a thin gingival biotype\n* Gingival recessions where a white colored implant is a great advantage\n* For patients with a titanium intolerance\u002Fsensitivity\n* For patients who prefer a bio-holistic\u002Fmetal-free dental approach.\n\nToday, clinicians are asking tor long-term clinical results of zirconia as a dental implant material. Therefore, Z-Systems AG is conducting this zirconia dental implant registry. A registry design was chosen because it will capture long-term benefits\u002Frisks from clinical routine without patient selection.",[27],"2025-08-20",{"date":115,"type":35},"2025-08-28",{"date":117,"type":35},"2023-09-07",{"date":119,"type":21},"2029-09",{"name":121,"class":122},"Z-Systems","INDUSTRY",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":15,"sex":16,"minAge":130,"maxAge":131,"enrollmentInfo":132,"targetDuration":4,"studyType":22,"phases":134,"briefSummary":135,"conditions":136,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":43},"100599331","effect-of-crown-material-on-gingival-microbial-colonization-100599331","NCT07083102","Effect of Crown Material on Gingival Microbial Colonization","Effect of Crown Material on Gingival Microbial Colonization: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Age between 20 to 50 years.\n* Both male and female patients will be selected.\n* Good oral hygiene (Defined as a plaque index score ≤ 1 across all assessed surfaces and no visible calculus deposits)\n* Dentate patients require fixed prostheses for the first time on mandibular pre-molars and molars.\n* Patient with no history of any dental and bony pathosis (cysts, cancerous lesion).\n\nExclusion Criteria:\n\n* Untreated periodontal diseases\n* Xerostomia\n* Pregnancy, lactation\n* Smokers\n* Individuals with systemic conditions like diabetes and immunosuppressive diseases","20 Years","50 Years",{"count":133,"type":21},30,[24],"* Prior approval from SOD ethical committee has been received.\n* All patients presenting to the General OPD of School of Dentistry, Islamabad will be screened. Those patients who fulfill the criteria will be referred to the Prosthodontics department.\n* The patients will undergo detailed history and oral examination after informed consent (Annexure-A). Patients will undergo radiographic investigation and based on this information they will be selected for the study according to the exclusion and inclusion criteria.\n* Eligible participants will be randomly assigned to one of the following groups using a computer-generated sequence with allocation concealment via sealed opaque envelopes:\n\n  * Group A: Control group\n  * Group B: Full-coverage PFM crowns\n  * Group C: Full-coverage Zirconia crowns\n* Baseline gingival samples will be collected with the help of sterile swab from the target tooth region prior to prosthesis placement and at the follow-up visits i.e. 1, and 3 months; both for experimental groups and control group.\n* Microbial analysis will be conducted through culture techniques to quantify CFUs and identify species.\n* A summary of the micro-organisms, their incubation media, temperature and time is presented in the following table:\n\nTable 1: Summary of the micro-organisms, their incubation media, temperature and time Micro-organism Growth Media Temperature Incubation time Candida albicans Saboraud Agar 370C 24-48 hours Streptococcus mutans BHI broth 370C 24-48 hours Staphylococcus aureus BHI broth 370C 24-48 hours Porphyromonas gingivalis BHI broth 370C 18-24 hours\n\n* Alongside, the same sample from sterile swabs will be smeared by fixating it on a microscopic slide and then Candida albicans will be stained by Periodic Acid Schiff technique, and the bacterial species using Gram staining.\n* All participants will receive standardized verbal and written instructions oral hygiene instructions to control for hygiene-related variation",[137,27],"Microbial Colonization","2025-07-16",{"date":140,"type":35},"2025-07-24",{"date":142,"type":21},"2025-08-15",{"date":144,"type":21},"2025-12-15",{"name":146,"class":147},"Pakistan Institute of Medical Sciences","OTHER_GOV",{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":155,"enrollmentInfo":156,"targetDuration":4,"studyType":22,"phases":157,"briefSummary":158,"conditions":159,"keywords":160,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":43},"100580468","enhancing-soft-tissues-around-inserted-implants-by-two-different-methods-100580468","NCT06837688","Enhancing Soft Tissues Around Inserted Implants by Two Different Methods","Evaluation of Xenogeneic Collagen Matrix Versus Connective Tissue Graft to Enhance Soft Tissue Profile Around Single Dental Implants in the Aesthetic Zone","Inclusion Criteria:\n\n* Aged 18 years or older.\n* Good oral hygiene, defined as full-mouth plaque score ≤25%.\n* Having a single missing tooth in the aesthetic zone of the maxilla.\n* Tooth extraction occurred at least 3 months prior to enrolment.\n* Having adequate bone volume for implant placement (bucco-palatal bone dimension of at least 6 mm).\n* Having at least 5 mm of keratinized tissue width at the implant site.\n\nExclusion Criteria:\n\n* Systemic diseases.\n* Smoking.\n* Periodontal disease.\n* Untreated caries lesions.\n* Need for horizontal bone augmentation at the time of implant placement.","60 Years",{"count":133,"type":21},[24],"This randomized controlled clinical trial investigates the efficacy of xenogeneic collagen matrix (XCM) versus autogenous subepithelial connective tissue graft (SCTG) in enhancing the peri-implant soft tissue profile around single dental implants in the aesthetic zone of the anterior maxilla. Thirty adult patients with a single missing tooth, adequate bone volume, and sufficient keratinized tissue will be recruited at Damascus University. Each patient will undergo a fully digital workflow for implant planning-including CBCT imaging, intraoral scanning, and CAD\u002FCAM fabrication of a surgical guide and provisional restoration-to ensure precision in implant placement. Immediately following implant insertion, patients will be randomly allocated (1:1) to either receive a CTG harvested from the palatal mucosa using a single incision technique or an XCM (Mucoderm®, Botiss Biomaterials) that is adapted and secured to the buccal mucosa. The primary outcome is the increase in buccal soft tissue profile, measured via superimposed digital surface models at baseline, immediately postoperatively, and at 3 months. Secondary outcomes include patient-reported measures (pain, edema, aesthetic satisfaction), clinical parameters (keratinized tissue width, soft tissue height), peri-implant health assessments, and radiographic assessment. By comparing these two methods, the study aims to determine whether the less invasive XCM can offer outcomes comparable to the CTG standard while reducing donor site morbidity and overall surgical time.",[27],[161,162,163],"Peri-implant soft tissue augmentation","Xenogeneic collagen matrix","Connective tissue graft","2025-03-03",{"date":166,"type":35},"2025-03-05",{"date":168,"type":35},"2025-03-01",{"date":170,"type":21},"2026-12-31",{"name":172,"class":42},"Damascus University",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":4,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":180,"targetDuration":109,"studyType":110,"phases":4,"briefSummary":182,"conditions":183,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":192},"100472063","post-market-clinical-follow-up-pmcf-medical-device-registry-of-z-systems-zirconia-dental-products-z-systems-registry-100472063","NCT05427006","Post Market Clinical Follow Up (PMCF) Medical Device Registry of Z-Systems Zirconia Dental Products: Z-Systems Registry","Post Market Clinical Follow Up (PMCF) Medical Device Registry of Z-Systems Zirconia Dental Products: Z-Systems Registry Z-Systems Sub-Registry Plan: Z5-BL Dental Implants Z-Systems Sub-Registry Plan: Z5-TL Dental Implants","Inclusion Criteria:\n\n* Adult patient (≥ 18 years) was or will be implanted with up to 5 implants of the Z-Systems Z5-BL or Z5-TLproduct group\n* Patient has signed Informed Consent.\n\nExclusion Criteria:\n\n* None",{"count":181,"type":21},240,"Commercially pure (CP) titanium is the gold standard to produce dental implants because it has a huge volume of scientific publications over a period of more than 50 years, it is cheap and simple to produce (i.e., making dental implants economically \"affordable\") and comes in numerous specific designs of screws for various indications. That is why more than 95% of the implant market is dominated by titanium.\n\nHowever, there is an innovation trend to manufacture implants from more inert and biocompatible materials. Ceramic implants represent a valuable alternative for expanding the patient base of clinicians, especially in cases with challenging aesthetic demand. Furthermore, there has been a significant increase in the number of patients requesting metal-free dentistry or bio-holistic implant treatments.\n\nIn the past, ceramics were often branded as \"inferior\" quality due to its reputation as being brittle but the growing volume of scientific publications specifically on zirconia are demonstrating that it is comparable in fracture-strength with titanium implants. There is a clear market niche for zirconia implants, especially in cases of:\n\n* Aesthetic reconstructions in the anterior region, especially in patients with a thin gingival biotype\n* Gingival recessions where a white colored implant is a great advantage\n* For patients with a titanium intolerance\u002Fsensitivity\n* For patients who prefer a bio-holistic\u002Fmetal-free dental approach.\n\nToday, clinicians are asking for long-term clinical results of zirconia as a dental implant material. Therefore, Z-Systems AG is conducting this zirconia dental implant registry. A registry design was chosen because it will capture long-term benefits\u002Frisks from clinical routine without patient selection.",[27],"2025-01-23",{"date":186,"type":35},"2025-01-28",{"date":188,"type":35},"2022-07-01",{"date":190,"type":21},"2028-09",{"name":121,"class":122},5,{"id":194,"slug":195,"hasResults":11,"nctId":196,"briefTitle":197,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":199,"targetDuration":201,"studyType":110,"phases":4,"briefSummary":202,"conditions":203,"keywords":207,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":43},"100419452","outcome-of-dental-implant-therapy-in-patients-treated-with-antiresorptive-medication-100419452","NCT04741906","Outcome of Dental Implant Therapy in Patients Treated With Antiresorptive Medication","Inclusion Criteria:\n\n* Patient with cancer or osteoporosis, treated with antiresorptive treatment.\n* The patients should have sufficient compliance, this includes willingness to have the planned assessments\n* The patient should have an expected life span at enrollment of at least 2 years.\n* The local bone quality and quantity should be sufficient for implant insertion without bone augmentation and is classified according to the classification by Cawood \\& Howell 1988.\n\nExclusion Criteria:\n\n* \\> 10 cigarettes daily\n* HbA1c \\> 53 mmol\u002Fmol\n* Poor oral hygiene\n* Poor general condition: ECOG score 3 or 4.\n* Poor prognosis: Expected survival \\\u003C2 year is an exclusion cause.\n* Presence of metastases of the liver brain.\n* Poor local jaw bone quality acc. to Cawood classification stage 3 or 4.\n* Unwillingness to comply with the planned assessments and recordings",{"count":200,"type":21},225,"2 Years","Aim of the study is to examine the feasibility of dental implant insertion in patients receiving high, adjuvant and low dose \\> 4 years.",[27,204,205,206],"Implants","Cancer","Osteoporosis",[208,209,210,211,212,213,214,215,216],"Dental implants","High dose antiresorptive medication","Rehabilitation","Denosumab","Bisphosphonate","Oral rehabilitation","Adjuvant dose antiresorptive medication","Low dose antiresorptive medication","Bone modifying agents","2024-08-20",{"date":219,"type":35},"2024-08-21",{"date":221,"type":35},"2017-08-01",{"date":223,"type":21},"2025-12-31",{"name":225,"class":42},"Copenhagen University Hospital at Herlev",{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":232,"eligibilityCriteria":233,"healthyVolunteers":15,"sex":16,"minAge":234,"maxAge":4,"enrollmentInfo":235,"targetDuration":4,"studyType":22,"phases":237,"briefSummary":238,"conditions":239,"keywords":241,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":43},"100417293","two-unit-cantilever-implant-prostheses-made-of-monolithic-zirconia-or-pfm-100417293","NCT04713800","Two-unit Cantilever Implant Prostheses Made of Monolithic Zirconia or PFM","Randomized Controlled Clinical Trial of Two-unit Cantilever Implant Prostheses Made of Monolithic Zirconia on Titanium Base Abutments or Porcelain-fused to Metal on Gold Abutments","Cantilever","Inclusion Criteria:\n\n* Minimal age of 22 years old.\n* No general medical condition which represents a contraindication to implant treatment\n* Good oral hygiene (PII ≤ 20%), and healthy periodontal tissues (BOP≤ 20%)\n* Two adjacent-teeth gap in posterior maxilla or mandible arch (first premolar, second premolar, first molar, second molar) with an osseointegrated regular or wide-diameter bone-level implant in a prosthetically correct position to allow occlusal screw-retention. Free-end edentulous gaps can also be included\n* Presence of antagonist occlusal units\n\nExclusion Criteria:\n\n* Severe bruxism or clenching habits\n* Patients with inadequate oral hygiene or persistent intraoral infection\n* Women who are pregnant or breast feeding at the day of inclusion\n* Smokers exceeding 15 cigarettes \u002F day, or equivalent; patients chewing tobacco\n* Unable or unwilling to cooperate for the trial period\n* Estimated cantilever crown mesial-distal length \\> 10 mm\n* Estimated implant crown height (from implant platform to occlusal contact points) \\> 15 mm","22 Years",{"count":236,"type":21},38,[24],"The aim of is to compare the survival rate and technical outcomes of cantilever implant-supported fixed denture prosthetics (cFDPs) made either out of monolithic zirconia bonded to a titanium base in a digital workflow, or porcelain fused-to metal using a gold abutment in a conventional workflow. In addition, biological outcomes, wear patterns, PROMs and time efficiency will be recorded. The null hypothesis is: the reconstruction type does not influence the survival rate and technical outcomes of 2-unit implant-supported cFDP.",[240,27],"Jaw, Edentulous, Partially",[242,232,243,244,245,246,247],"Dental Implants","Titanium base","Dental abutment","Fixed dental prosthesis","Monolithic zirconia","Porcelain fused to metal","2022-11-21",{"date":250,"type":35},"2022-11-23",{"date":252,"type":35},"2021-07-28",{"date":254,"type":21},"2027-07",{"name":256,"class":42},"University of Geneva, Switzerland"]