[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"October University for Modern Sciences and Arts\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":337},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,37,69,102,135,163,191,218,247,269,291,313],{"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":4,"briefSummary":13,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":4},"100636124","correlation-between-posterior-crossbite-and-risk-of-obstructive-sleep-apnea-100636124",false,"NCT07561606","Correlation Between Posterior Crossbite and Risk of Obstructive Sleep Apnea","Correlation Between Posterior Crossbite and Risk of Obstructive Sleep Apnea: A Questionnaire-Based Analysis","Inclusion Criteria:\n\n* Children in mixed dentition stage aged 6-12 years\n* Presence of posterior crossbite\n\nExclusion Criteria:\n\n* Syndromic patients\n* Previous orthodontic treatment\n* Chronic respiratory or neurological disorders Matching criteria and allocation ratio","ALL","6 Years","12 Years",{"count":20,"type":21},420,"ESTIMATED","OBSERVATIONAL",[24],"Crossbite Teeth","NOT_YET_RECRUITING","2026-04-25",{"date":28,"type":29},"2026-05-01","ACTUAL",{"date":31,"type":21},"2026-04",{"date":33,"type":21},"2026-06",{"name":35,"class":36},"October University for Modern Sciences and Arts","OTHER",{"id":38,"slug":39,"hasResults":11,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":4,"eligibilityCriteria":43,"healthyVolunteers":11,"sex":16,"minAge":44,"maxAge":45,"enrollmentInfo":46,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":67,"locationsCount":68},"100626604","clinical-and-radiographic-assessment-of-neo-putty-mta-versus-formocresol-used-in-vital-pulpotomy-of-mandibular-primary-molars-100626604","NCT07437794","Clinical and Radiographic Assessment of Neo Putty MTA Versus Formocresol Used in Vital Pulpotomy of Mandibular Primary Molars","Clinical and Radiographic Assessment of Neo Putty MTA Versus Formocresol Used in Vital Pulpotomy of Mandibular Primary Molars: A Randomized Clinical Trial","Inclusion Criteria:\n\nChildren with asymptomatic decayed primary mandibular molar(s).\n\n* Patient and parent showing cooperation and compliance.\n* Children 4-9 years old.\n* Vital carious primary(s) with complete root formation.\n* Asymptomatic teeth or without clinical symptoms of spontaneous pain.\n* No clinical evidence of pulp degeneration like the history of spontaneous or nocturnal pain, tenderness to percussion, pathologic tooth mobility, swelling, or fistulous tract.\n* Both genders will be included.\n* No radiographic evidence of pulp degeneration such as internal root resorption, external root resorption, or furcal radiolucency.\n* Presence of two thirds of the root.\n* Teeth that can be restored.\n* Children with prior parental consent.\n\nExclusion Criteria:\n\n* History of any systemic disease.\n* Hemostasis is not achieved within 5 minutes of pulp amputation, by direct contact with a wet cotton pellet before the material placement.\n* The remaining radicular tissue was non-vital (with suppuration or purulence necrosis).","4 Years","9 Years",{"count":47,"type":21},68,"INTERVENTIONAL",[50],"NA","This randomized clinical trial aims to evaluate the clinical and radiographic success of NeoPutty MTA compared to formocresol in vital pulpotomy of mandibular primary molars in children aged 4 to 9 years. Participants will be randomly allocated into two groups (1:1) to receive pulpotomy using either NeoPutty MTA or formocresol, followed by restoration with stainless steel crowns. Clinical and radiographic outcomes will be assessed during follow-up visits.",[53],"Deep Caries in Primary Molars",[53,55,56,57,58,59,60],"NeoPutty MTA","Mineral Trioxide Aggregate","Formocresol","Vital Pulp Therapy","Pulpotomy","Stainless Steel Crown","2026-02-23",{"date":63,"type":29},"2026-02-27",{"date":65,"type":21},"2026-03-01",{"date":28,"type":21},{"name":35,"class":36},1,{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":48,"phases":80,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":68},"100626171","artificial-intelligence-versus-conventional-digital-design-for-fixed-dental-prosthesis-100626171","NCT07432165","Artificial Intelligence Versus Conventional Digital Design for Fixed Dental Prosthesis","Accuracy Assessment of Artificial Intelligence Versus Conventional Digital Design for Fixed Dental Prosthesis: (An Invitro Study)","Inclusion Criteria:\n\n* Adults aged 18-65 years Patients with a damaged tooth requiring a fixed dental prosthesis Available digital intraoral scans Adequate occlusal anatomy for analysis of opposing teeth\n\nExclusion Criteria:\n\n* Incomplete or poor-quality digital scans Severe occlusal abnormalities affecting analysis Patients outside the specified age range","18 Years","65 Years",{"count":79,"type":21},1000,[50],"This in vitro study aims to evaluate the accuracy of an Artificial Intelligence (AI)-based automatic design system for fixed dental prosthesis (FDP) compared with conventional computer-aided design (CAD) software. Digital scans of teeth requiring fixed dental prosthesis will be collected and used to generate prosthetic designs using two approaches: human-designed CAD restorations and AI-generated restorations.\n\nThe primary outcome is design accuracy assessed using 3D superimposition and Intersection over Union (IOU) percentage. Secondary outcomes include margin detection performance measured using F1 score, precision, and recall. A total sample size of 438 scans will be analyzed.\n\nThe study will determine whether AI-generated prosthesis designs demonstrate comparable accuracy to conventional digital designs.",[83],"Accuracy of Artificial Intelligence in Fixed Dental Prosthesis Design",[85,86,87,88,89,90,91,92],"Artificial Intelligence","CAD\u002FCAM","Fixed Dental Prosthesis","Dental Crown Design","3D Superimposition","Deep Learning","Generative Adversarial Network (GAN)","Prosthodontics","RECRUITING","2026-02-19",{"date":96,"type":29},"2026-02-25",{"date":98,"type":29},"2025-06-15",{"date":100,"type":21},"2026-06-17",{"name":35,"class":36},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":109,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":48,"phases":113,"briefSummary":114,"conditions":115,"keywords":117,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":68},"100623343","evaluation-of-zinc-oxide-eugenol-and-iodoform-calcium-hydroxide-as-filling-materials-in-primary-molar-root-canals-prepared-by-rotary-and-manual-files-100623343","NCT07395401","Evaluation of Zinc Oxide Eugenol and Iodoform-Calcium Hydroxide as Filling Materials in Primary Molar Root Canals Prepared by Rotary and Manual Files","Clinical and Radiographic Evaluation of Zinc Oxide Eugenol (ZOE) and Iodoform-Calcium Hydroxide (Metapex) as Filling Materials in Primary Molar Root Canals Prepared by Rotary and Manual Files: (Randomized Control Trial Study)","Inclusion Criteria:\n\n1. Apparently healthy cooperative children indicated for partial pulpectomy.\n2. Restorable primary molars.\n3. No mobility, or external pathological root resorption.\n\nExclusion Criteria:\n\n1. Uncooperative children.\n2. Children with systemic medical illness.\n3. More than 2\u002F3 of root resorbed.","5 Years","8 Years",{"count":112,"type":21},44,[50],"This randomized controlled clinical trial aims to compare the clinical and radiographic outcomes of Zinc Oxide Eugenol (ZOE) and Iodoform-Calcium Hydroxide (Metapex) as root canal filling materials in primary molars prepared using either rotary or manual instrumentation techniques. Forty-four teeth from children aged 5-8 years indicated for pulpectomy will be randomly allocated into four equal groups based on the combination of instrumentation method and filling material. Clinical parameters-pain, mobility, and sensitivity-will be assessed using standardized scales, while radiographic outcomes, including root resorption and bone density, will be evaluated using Cone Beam Computed Tomography (CBCT) at baseline, 6 months, and 12 months. The study seeks to determine which obturation material and canal preparation technique yield superior healing, adaptation, and resorption compatible with the physiological process of primary tooth exfoliation. Findings are expected to inform evidence-based selection of endodontic materials and instrumentation methods in pediatric dentistry.",[116],"Carious Primary Molars Indicated for Pulpectomy",[118,119,120,121,122,123,124,125,126],"Iodoform-Calcium Hydroxide","Metapex","Zinc Oxide Eugenol","Manual Instrumentation Method","Rotary Instrumentation Method","pulpectomy","primary molars","radiographic assessment","clinical assessment","2026-02-01",{"date":129,"type":29},"2026-02-09",{"date":131,"type":21},"2026-02-15",{"date":133,"type":21},"2026-03-15",{"name":35,"class":36},{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":142,"targetDuration":4,"studyType":48,"phases":144,"briefSummary":145,"conditions":146,"keywords":149,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":68},"100621205","lavender-vs-bitter-orange-aromatherapy-to-reduce-anxiety-and-pain-in-pediatric-local-anesthesia-100621205","NCT07367594","Lavender vs Bitter Orange Aromatherapy to Reduce Anxiety and Pain in Pediatric Local Anesthesia","Comparative Evaluation of the Effect of Lavender Versus Bitter Orange Essential Oils Aromatherapy on Decreasing Dental Anxiety and Pain of Children During Administration of Local Anesthetic: (A Randomized Clinical Trial)","Inclusion Criteria:\n\n* Children with the age range of 6-12 years\n* Any dental procedure that requires injection of local anesthesia.\n* Cooperative patients.(according to Frankl's classification class 1 and 2)\n* Parents or guardians willing to participate in the study.\n* Healthy child\n\nExclusion Criteria:\n\n* Children with complicated systemic disease.\n* Uncooperative patients. .(according to Frankl's classification class 3 and 4)\n* Children with severe cognitive impairment or developmental disorders\n* Children with respiratory tract infections.\n* Children experiencing dental pain such as (acute pain or hyperemia).",{"count":143,"type":21},26,[50],"This randomized controlled clinical trial aims to evaluate and compare the effectiveness of lavender essential oil and bitter orange essential oil aromatherapy in reducing dental anxiety and pain in children during the administration of local anesthesia. Children aged 6-12 years undergoing dental procedures requiring local anesthetic infiltration will be randomly assigned to lavender aromatherapy, bitter orange aromatherapy, or placebo (empty inhaler). Dental anxiety will be assessed using pulse rate and blood pressure measurements, while pain will be evaluated using the FLACC behavioral pain scale. The findings are expected to provide evidence on the role of aromatherapy as a non-pharmacological, safe, and cost-effective behavior guidance method in pediatric dentistry.",[147,148],"Dental Anxiety","Local Anesthesia",[150,151,152,153,154],"aromatherapy","local anesthesia injection","lavender essential oil","bitter orange essential oil","dental anxiety","2026-01-26",{"date":157,"type":29},"2026-01-28",{"date":159,"type":21},"2026-02",{"date":161,"type":21},"2026-04-01",{"name":35,"class":36},{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":4,"eligibilityCriteria":169,"healthyVolunteers":11,"sex":16,"minAge":170,"maxAge":109,"enrollmentInfo":171,"targetDuration":4,"studyType":48,"phases":173,"briefSummary":174,"conditions":175,"keywords":178,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":190,"locationsCount":68},"100622332","efficacy-of-silver-diamine-fluoride-versus-nano-silver-fluoride-in-arresting-active-dentin-caries-in-primary-teeth-in-young-children-100622332","NCT07382245","Efficacy of Silver Diamine Fluoride Versus Nano-Silver Fluoride in Arresting Active Dentin Caries in Primary Teeth in Young Children","Efficacy of Silver Diamine Fluoride Versus Nano-Silver Fluoride in Arresting Active Dentin Caries in Primary Teeth in Young Children: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Apparently healthy children.\n* Children with age ranged from 3-5 years from both genders.\n* Children who refused dental treatment with Frankl Behavior Rating Scale 1 and 2.\n* Children having molars with active dentin caries score (2,3,4) according to International Caries Detection and Assessment System- ICDAS II, detected by visual and tactile.\n* Parents\u002Fguardians accept treatment and write informed consent.\n\nExclusion Criteria:\n\n* Children with allergy to silver from their medical history.\n* Children with ulcerative gingivitis.\n* Children with primary molars with the following criteria:\n* Symptomatic\n* Involving the pulp\n* Presence of fistula or sinus\n* Presence of gingival inflammation and Pain on percussion\n* Close to exfoliation","3 Years",{"count":172,"type":21},60,[50],"Early childhood caries is a major public health problem affecting preschool children worldwide. Silver Diamine Fluoride is a well-established non-invasive treatment for arresting caries; however, it causes black discoloration of treated lesions. Nano-Silver Fluoride has been introduced as an alternative that may arrest caries without discoloration.\n\nThis randomized clinical trial aims to compare the efficacy of Silver Diamine Fluoride and Nano-Silver Fluoride in arresting active dentin caries in primary teeth and to assess discoloration, post-operative pain, and parental satisfaction over a 12-month follow-up period.",[176,177],"Early Childhood Caries (ECC)","Active Dentin Caries in Primary Molars",[179,180,181,182,183],"Early Childhood Caries","primary molar","Nano-Silver Fluoride","Silver Diamine Fluoride","SDF","2026-01-25",{"date":186,"type":29},"2026-02-02",{"date":188,"type":21},"2026-01-30",{"date":133,"type":21},{"name":35,"class":36},{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":196,"acronym":4,"eligibilityCriteria":197,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":198,"targetDuration":4,"studyType":48,"phases":200,"briefSummary":201,"conditions":202,"keywords":204,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":214,"startDateStruct":215,"completionDateStruct":216,"leadSponsor":217,"locationsCount":68},"100621725","preemptive-analgesia-for-pain-and-anxiety-control-in-children-with-mih-100621725","NCT07374354","Preemptive Analgesia for Pain and Anxiety Control in Children With MIH","Assessment of Preemptive\u002FPreoperative Analgesia Effect on Pain Perception and Anxiety Management in Children With Molar Incisor Hypo-Mineralization During Restorative Treatment of First Permanent Molar: A Triple-Blinded Randomized Clinical Trial.","Inclusion Criteria:\n\n1. Patient with molar incisor hypo-mineralization.\n2. Patient's age ranges from 6 to 12 years old.\n3. The affected tooth has demarcated opacity with post eruptive enamel breakdown.\n4. No cavitated lesion is related to the defect of previous restorative or preventive treatment.\n\nExclusion Criteria:\n\n1. Children who are physically or mentally disabled or having any medical condition that will affect or complicate assessment of the intervention.\n2. Loss of tooth structure due to caries.\n3. intolerance to ibuprofen.\n4. developmental defects, including amelogenesis imperfecta and dentinogenesis imperfecta.",{"count":199,"type":21},46,[50],"This randomized, triple-blinded clinical trial aims to evaluate the effect of preemptive analgesia using ibuprofen on pain perception and anxiety during restorative treatment of first permanent molars in children diagnosed with molar-incisor hypomineralization (MIH). MIH-affected teeth often present with hypersensitivity, difficulty in achieving adequate anesthesia, and increased dental anxiety, which complicates dental treatment. Participants aged 6-12 years with MIH will receive either ibuprofen syrup or placebo 30 minutes before treatment. Pain will be assessed using the FLACC Behavioral Pain Scale and Wong-Baker FACES scale, and anxiety will be evaluated through heart rate and oxygen saturation. The results will determine whether preoperative ibuprofen reduces intraoperative pain and improves anxiety control in this population.",[203],"Pain and Anxiety in Children With MIH",[205,206,207,208,147,209,210,211,212,213],"Molar Incisor Hypomineralization (MIH)","Preemptive Analgesia","Ibuprofen","Dental Pain","FLACC Scale","Wong-Baker FACES","Post-Eruptive Enamel Breakdown","Children 6-12 Years","Analgesic Efficacy",{"date":157,"type":29},{"date":159,"type":21},{"date":127,"type":21},{"name":35,"class":36},{"id":219,"slug":220,"hasResults":11,"nctId":221,"briefTitle":222,"officialTitle":223,"acronym":4,"eligibilityCriteria":224,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":225,"targetDuration":4,"studyType":48,"phases":227,"briefSummary":228,"conditions":229,"keywords":231,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":244,"leadSponsor":245,"locationsCount":246},"100611780","effectiveness-of-virtual-reality-vs-show-do-technique-on-dental-anxiety-in-children-with-hearing-impairment-100611780","NCT07245030","Effectiveness of Virtual Reality vs Show-Do Technique on Dental Anxiety in Children With Hearing Impairment","A Comparative Evaluation of the Effectiveness of Virtual Reality Eyewear vs Show-Do Technique on Dental Anxiety and Behavior in a Group of Children With Different Levels of Hearing Impairment During Dental Prophylaxis Procedure: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Children with moderate to severe Hearing impairment.\n2. Children require dental prophylaxis.\n3. Apparently, Health Children.\n\nExclusion Criteria:\n\n1. Children with severe cognitive impairment or developmental disorders.\n2. Children who are unable or unwilling to cooperate with the study protocol or assessment.\n3. Children with complicated systemic diseases.",{"count":226,"type":21},54,[50],"This randomized controlled clinical trial aims to compare the effectiveness of virtual reality (VR) eyewear used as a distraction method in combination with the Show-Do (SD) technique versus the traditional Show-Do technique alone in managing dental anxiety and improving behavioral responses among Egyptian children with different levels of hearing impairment during a dental prophylaxis procedure. The study will evaluate dental anxiety using pulse rate and the PJS-Pictorial Scale, while behavior will be assessed using the Frankl Behavior Rating Scale. The trial seeks to provide evidence-based guidance on the implementation of VR technology as an adjunctive non-pharmacological tool for children with communication barriers in pediatric dentistry.",[230],"Dental Anxiety of Hearing Impairment",[232,233,234,235,236,237,238,239],"dental prophylaxis procedure","scaling","polishing","oral hygiene instructions","virtual reality","Anxiety","behavioral","hearing impairment","2025-11-20",{"date":242,"type":29},"2025-11-24",{"date":240,"type":21},{"date":127,"type":21},{"name":35,"class":36},2,{"id":248,"slug":249,"hasResults":11,"nctId":250,"briefTitle":251,"officialTitle":252,"acronym":253,"eligibilityCriteria":254,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":4,"enrollmentInfo":255,"targetDuration":4,"studyType":48,"phases":257,"briefSummary":258,"conditions":259,"keywords":4,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":261,"lastUpdatePostDateStruct":262,"startDateStruct":264,"completionDateStruct":266,"leadSponsor":268,"locationsCount":68},"100606376","non-submerged-de-epithelialized-free-gingival-graft-versus-conventional-free-gingival-graft-100606376","NCT07174752","Non-Submerged De-Epithelialized Free Gingival Graft Versus Conventional Free Gingival Graft","Esthetic Evaluation of Non-Submerged De-Epithelialized Free Gingival Graft (Ns-dFGG) Versus Conventional Free Gingival Graft (cFGG) for the Augmentation of The Keratinized Mucosa: Randomized Controlled Clinical Trial","Ns-dFGG; cFGG","Inclusion Criteria:\n\n* Adult patients: 18-60.\n* Insufficient width of keratinized mucosa, that is less than 2 mm.\n* Lower anterior areas.\n* Good oral hygiene.\n\nExclusion Criteria:\n\n* Systemic conditions that prevent the patient from undergoing minor oral surgical procedures or hinder the healing process.\n* Patient undertaking radiotherapy or chemotherapy.\n* Smokers.\n* Pregnant females",{"count":256,"type":21},30,[50],"The goal of this (study type: RCT) is to learn if the use of the non-submerged de-epithelized FGG will result in better esthetic outcomes in adults. The main questions that it aims to answer are:\n\n* Does this procedure increase the width of keratinized tissue?\n* Does this procedure increase the depth of the vestibule? Researchers will compare this technique with the gold standard using the FGG to evaluate which technique provides better esthetics.",[260],"Deficient Keratinized Mucosa","2025-09-15",{"date":263,"type":29},"2025-09-16",{"date":265,"type":29},"2024-12-29",{"date":267,"type":21},"2026-12-29",{"name":35,"class":36},{"id":270,"slug":271,"hasResults":11,"nctId":272,"briefTitle":273,"officialTitle":274,"acronym":4,"eligibilityCriteria":275,"healthyVolunteers":276,"sex":16,"minAge":44,"maxAge":45,"enrollmentInfo":277,"targetDuration":4,"studyType":48,"phases":278,"briefSummary":279,"conditions":280,"keywords":4,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":283,"lastUpdatePostDateStruct":284,"startDateStruct":286,"completionDateStruct":288,"leadSponsor":290,"locationsCount":68},"100538257","clinical-and-radiographic-evaluation-of-vital-pulpotomy-techniques-in-primary-molars-using-of-premixed-bioactive-bioceramic-mta-neo-putty-as-a-novel-pulpotomy-medication-versus-formocresol-100538257","NCT06288477","Clinical and Radiographic Evaluation of Vital Pulpotomy Techniques in Primary Molars Using of Premixed Bioactive Bioceramic MTA (Neo-putty) as a Novel Pulpotomy Medication Versus Formocresol","Clinical and Radiographic Evaluation of Vital Pulpotomy Techniques in Primary Molars Using of Premixed Bioactive Bioceramic MTA (Neo-putty) as a Novel Pulpotomy Medication Versus Formocresol: A Randomized Clinical Trial.","Criteria The eligibility criteria were set according to the guidelines of AAPD, 2020. (4)\n\nInclusion Criteria:\n\n1. 4 -9 years old\n2. Primary molars with no spontaneous or provoked pain\n3. Primary molars with at least two-thirds of the root length were still present.\n4. Primary molars with no sign of internal or other kinds of root or bone resorption.\n\nExclusion Criteria:\n\n1. Patients with systemic diseases (congenital or rheumatic heart disease, hepatitis, nephritis, tumor, cyclic neutropenia, leukemia, and children on long-term corticosteroid therapy).\n2. Un-cooperative patients.\n3. Un-restorable primary molars (Grossly broken-down primary molars that have decay extending way under the gingiva and tooth with root caries).",true,{"count":112,"type":21},[50],"Despite the benefit of formocresol, there are toxic effects allergic reactions and local soft and hard tissue necrosis have been reported when such formaldehyde compounds were used clinically, however, the adverse effect of the clinically used of this compound are not widely reported. It has been stated that it has a side effect on the permanent successor although it results as a successful technique for the treatment of the primary teeth",[281,59,282],"Vital","Techniques","2024-12-18",{"date":285,"type":29},"2024-12-20",{"date":287,"type":29},"2024-03-20",{"date":289,"type":21},"2025-02-01",{"name":35,"class":36},{"id":292,"slug":293,"hasResults":11,"nctId":294,"briefTitle":295,"officialTitle":296,"acronym":4,"eligibilityCriteria":297,"healthyVolunteers":276,"sex":16,"minAge":298,"maxAge":4,"enrollmentInfo":299,"targetDuration":4,"studyType":48,"phases":301,"briefSummary":302,"conditions":303,"keywords":4,"overallStatus":93,"whyStopped":4,"lastUpdateSubmitDate":305,"lastUpdatePostDateStruct":306,"startDateStruct":308,"completionDateStruct":310,"leadSponsor":312,"locationsCount":246},"100571206","digital-conventional-and-biomimetic-approaches-for-restoring-endodontically-treated-teeth-100571206","NCT06717230","Digital, Conventional, And Biomimetic Approaches for Restoring Endodontically Treated Teeth","Evaluating The Clinical Success And Patient Satisfaction of Digital, Conventional, And Biomimetic Approaches For Restoring Endodontically Treated Teeth: Randomized Controlled Trial.","Inclusion Criteria:\n\n* Endodontically-treated molar tooth with significant loss of tooth structure (both marginal ridges lost) requiring cuspal coverage.\n* Patients aged ≥15 years.\n* Controlled dental disease - no active caries or periodontal diseases\n* Patients will be available to be clinically reviewed up to 1 year\n\nExclusion Criteria:\n\n* Patients with poor oral hygiene.\n* Teeth with extensive cracks or fractures.\n* Deep subgingival margins (\\>0.5mm subgingival).\n* Non-restorable teeth.\n* Non-functional teeth (no opposing dentition).\n* Pocket probing depth \\> 3mm.\n* Mobility.\n* Patients with bruxism.","15 Years",{"count":300,"type":21},42,[50],"Endocrowns are preferred over the post-retained crown, especially at a young age for many reasons; they allow better gingival health and care due to placement of the supragingival margin, have greater fracture resistance limiting the risk for root fracture, thus improving the long-term prognosis of ETMs and has a superior ability to restore ETMs with short crowns, calcified root canals, and thin roots. Furthermore, using CAD\u002FCAM technology facilitates Endocrowns preparation making it simpler with less invasive techniques that can be prepared, fabricated, and cemented in a single visit. The high demand for permanent, esthetic, and conservative restorations has directed clinicians to restore permanent ETMs at a young age with Endo crowns as final coronal restorations.\n\nIn addition, Biomimetic dentistry leverages modern materials to replicate the biological and mechanical functions of natural teeth, presenting a distinct approach that minimizes the need for extensive tooth reduction and post-placement, particularly advantageous for endodontically treated teeth. Utilizing fiber-reinforced composites, this technique aims to strengthen the dentin-resin bond and evenly distribute occlusal forces across the restoration. By closely adhering to the intact tooth's natural contours and functionality, biomimetic restorations not only preserve more of the natural tooth structure but also reduce stress and strain within the restored tooth. This approach enhances longevity and minimizes the risk of bond failure, with any necessary repairs being straightforward and contributing to the restoration's sustainability. This study explores the application of fiber-reinforced composites within a biomimetic framework for restoring endodontically treated teeth, aiming to achieve durable and biologically compatible outcomes.",[304],"Endodontically Treated Teeth","2024-12-10",{"date":307,"type":29},"2024-12-16",{"date":309,"type":29},"2024-09-01",{"date":311,"type":21},"2025-10-01",{"name":35,"class":36},{"id":314,"slug":315,"hasResults":11,"nctId":316,"briefTitle":317,"officialTitle":318,"acronym":4,"eligibilityCriteria":319,"healthyVolunteers":276,"sex":16,"minAge":44,"maxAge":110,"enrollmentInfo":320,"targetDuration":4,"studyType":48,"phases":322,"briefSummary":323,"conditions":324,"keywords":326,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":329,"lastUpdatePostDateStruct":330,"startDateStruct":332,"completionDateStruct":334,"leadSponsor":336,"locationsCount":68},"100570755","evaluation-of-custom-designed-dental-storybook-on-the-dental-anxiety-and-behavior-of-children-100570755","NCT06711367","Evaluation of Custom-designed Dental Storybook on the Dental Anxiety and Behavior of Children","Comparative Evaluation of the Effectiveness of Custom-designed Dental Storybook Vs Tell Show Do on the Dental Anxiety and Behavior of Children: a Randomized Controlled Trial","Inclusion Criteria:\n\n* • Healthy children and children\u002Fparents can read and understand Arabic.\n\n  * The child needs an occlusal composite restoration.\n\nExclusion Criteria:\n\n* Children with special needs; children with a complete audiovisual impairment; children with\n* Learning difficulties or mental retardation.\n* Children who are not Arabic speakers.",{"count":321,"type":21},48,[50],"Conventional behavior management techniques, namely: verbal communication and tell-show-do were used in the operatory for the participating children (Group A). The children allocated in intervention group (Group B) received a costume-designed storybook explaining the diagnosis and procedures of occlusal composite restoration",[325,147],"Child Behavior",[327,328,154],"dental storybook","tell show do","2024-11-29",{"date":331,"type":29},"2024-12-02",{"date":333,"type":21},"2024-12-01",{"date":335,"type":21},"2025-05-02",{"name":35,"class":36},""]