[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100638282":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":45,"responsibleParty":68,"collaborators":26,"id":72,"slug":73,"hasResults":74,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":79,"sex":80,"minAge":81,"maxAge":26,"enrollmentInfo":82,"targetDuration":26,"studyType":85,"phases":86,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":48,"whyStopped":26,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"Universiti Teknologi Mara","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Group A: Control","PLACEBO_COMPARATOR","Monolithic zirconia screw retained crown conditioned with titanium standard healing abutment (SHA) and fabricated with standard monoscan body",[13],"Device: standard healing abutment",{"label":15,"type":16,"description":17,"interventionNames":18},"Group B: PEEK AHA","ACTIVE_COMPARATOR","Monolithic zirconia screw retained crown conditioned and fabricated with AHA digital workflow",[19],"Device: AHA PEEK",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","AHA PEEK","polyetheretherketone (PEEK) anatomic healing abutment versus standard anatomic healing abutment",[15],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"standard healing abutment","Titanium healing abutment",[9],[32],{"name":33,"affiliation":5,"role":34},"Professor Dr Mohd Yusmiaidil Putera Mohd Yusoff, phd","STUDY_DIRECTOR",[36,41],{"name":37,"role":38,"phone":39,"phoneExt":26,"email":40},"Nur Hafizah Kamar Affendi, master","CONTACT","+60361266545","hafizah_kamar@uitm.edu.my",{"name":42,"role":38,"phone":43,"phoneExt":26,"email":44},"NORWATI Atikah Mustafa, phd","0361266545","norwati_atikah@uitm.edu.my",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"Universiti Teknologi MARA","RECRUITING","Sungai Buloh","Selangor","42300","Malaysia","MY",{"type":55,"coordinates":56},"Point",[57,58],101.561,3.21,{"lat":58,"lon":57},[61,63,65],{"name":62,"role":38,"phone":43,"phoneExt":26,"email":40},"NUR HAFIZAH AFFENDI, MASTER",{"name":26,"role":38,"phone":26,"phoneExt":26,"email":64},"nfizakama@gmail.com",{"name":66,"role":67,"phone":26,"phoneExt":26,"email":26},"Nur Hafizah Kamar Affendi, MASTER","PRINCIPAL_INVESTIGATOR",{"type":69,"investigatorFullName":70,"investigatorTitle":71,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"SPONSOR_INVESTIGATOR","DR NUR HAFIZAH KAMAR AFFENDI","Assoc Prof","100638282","volumetric-analysis-of-peri-implant-soft-tissue-changes-between-polyethereketonepeek-anatomic-healing-abutments-and-standard-healing-abutments-in-posterior-single-implant-restorations-100638282",false,"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,"ALL","18 Years",{"count":83,"type":84},38,"ESTIMATED","INTERVENTIONAL",[87],"NA","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).",[90,91,92],"Peri-Implant Health","Peri-Implant Tissues","Soft Tissue Augmentation at Dental Implants",[91,94,95],"volumetric analysis","soft tissue","2026-05-31",{"date":98,"type":99},"2026-06-03","ACTUAL",{"date":101,"type":84},"2026-05-23",{"date":103,"type":84},"2028-10-01",{"name":70,"class":6},1]