[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Khyber College of dentistry\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":117},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,46,72,94],{"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":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100639347","comparasion-of-dental-anxiety-in-first-time-complete-denture-patients-100639347",false,"NCT07597057","Comparasion of Dental Anxiety in First Time Complete Denture Patients","Comparison of Dental Anxiety Level in Edentulous Patients Before and After Seeking Complete Denture Treatment for the First Time: A Quasi-Experimental Study","Inclusion Criteria: Edentulous patients (missing all teeth) requiring first-time complete dentures.\n\nExclusion Criteria: History of previous denture use, severe cognitive impairment, or systemic diseases contraindicating dental procedures.","ALL","40 Years","70 Years",{"count":20,"type":21},70,"ESTIMATED","INTERVENTIONAL",[24],"NA","This quasi-experimental study compares dental anxiety levels in edentulous patients at two specific clinical points: the primary impression appointment and the denture insertion appointment. The study aims to determine if the process of receiving first-time complete dentures significantly impacts patient anxiety levels. Data will be collected from 70 participants at the Khyber College of Dentistry over a five-week interval between the two appointments",[27,28],"Edentulous Mouth","Dental Anxiety",[30,31,32,33],"complete denture","dental anxiety scale","prosthodontics","edentulism","NOT_YET_RECRUITING","2026-05-13",{"date":37,"type":38},"2026-05-19","ACTUAL",{"date":40,"type":21},"2026-05-01",{"date":42,"type":21},"2026-12-30",{"name":44,"class":45},"Khyber College of dentistry","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":4},"100637011","hard-splint-vs-conservative-therapy-for-tmj-pain-management-100637011","NCT07573137","Hard Splint Vs Conservative Therapy for TMJ Pain Management","Efficacy of Hard Splint Vs Conservative Therapy in the Pain Management of Temporomandibular Joint Disorders","Inclusion Criteria:\n\n* Patients diagnosed with TMJ disorders based on clinical examination. Patients willing to participate and provide informed consent.\n\nExclusion Criteria:\n\n* Patient with a history of recent TMJ surgery or trauma. Patients with systemic joint diseases (e.g Rheumatoid Arthritis, Osteoporosis, Osteopetrosis, Osteomalacia).\n\nPatients currently using other occlusal appliances or undergoing active orthodontic treatment.","18 Years","60 Years",{"count":56,"type":21},60,[24],"The purpose of this study is to compare the efficacy of a hard occlusal splint versus conservative therapy (using topical Ibuprofen gel and counseling) in the management of patients with temporomandibular (TMJ) joint disorders. The study aims to determine which treatment is more effective at reducing pain, measured by Visual Analogue Scale (VAS), at 1 week and 4 weeks post therapy.",[60],"Temporomandibular Disorders (TMDs)",[62,63,64,65],"Hard Occlusal splint","Conservative therapy","Visual Analogue Scale","Facial pain",{"date":67,"type":38},"2026-05-15",{"date":40,"type":21},{"date":70,"type":21},"2026-11-30",{"name":44,"class":45},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":78,"sex":16,"minAge":53,"maxAge":17,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},"100602154","comparison-of-outcome-of-safe-t-separators-and-conventional-elastomeric-separators-100602154","NCT07119814","Comparison of Outcome of Safe T Separators and Conventional Elastomeric Separators","Inclusion Criteria:\n\n* Age range (18-40) Years Male\u002FFemale Patients undergoing fixed orthodontic treatment as mentioned in operational\n\nExclusion Criteria:\n\n* Patients with poor oral hygiene Patients with periodontal conditions Patients failed to provide consent form",true,{"count":80,"type":21},66,[24],"All participants in this study will be provided with information concerning the study's objectives, and benefits associated with participation. Participants will be informed that their involvement in this study presents no potential risks associated with their participation. Written consent will be obtained with appropriate information provided. Demographic data like age, BMI, gender, residence, socio economic status, occupation status, and literacy status will be documented. Patients undergoing fixed orthodontic treatment will be allocated in two groups equally by using the blocked randomization technique. Patients in Group A will undergo safe-T separators i.e initial thickness of Safe-T separators will be 1mm, Patients in Group B will undergo conventional elastomeric separators i.e thickness of elastomeric separators will be 1.2 mm. Separators will be positioned on either side of lower arch, each type of separator will be in sites, resulting in a sites within the lower arch. A separator placement tool will be utilised to position the separators. The comprehensive assessment will be carried out under the supervision of a consultant possessing at least five years of post-fellowship experience. Patient data will be recorded using a predefined structured proforma.",[84],"Malocclusion","2025-08-06",{"date":87,"type":38},"2025-08-13",{"date":89,"type":21},"2025-12-01",{"date":91,"type":21},"2026-04-15",{"name":44,"class":45},1,{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":78,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":101,"targetDuration":4,"studyType":22,"phases":103,"briefSummary":104,"conditions":105,"keywords":107,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":93},"100600683","this-study-will-assess-whether-the-treatment-provided-by-dentist-is-successful-in-meeting-the-expectations-of-patient-by-asking-questions-related-to-aesthetics-chewing-ability-comfort-and-phonetics-before-and-after-providing-treatment-and-the-patient-will-tell-through-visual-analog-scale-100600683","NCT07100678","This Study Will Assess Whether the Treatment Provided by Dentist is Successful in Meeting the Expectations of Patient by Asking Questions Related to Aesthetics, Chewing Ability, Comfort and Phonetics Before and After Providing Treatment and the Patient Will Tell Through Visual Analog Scale","Comparison Of Pretreatment Expectations and Posttreatment Satisfaction In Patients Receiving Porcelain-Fused-to-Metal Fixed Dental Prosthesis: A Quasi-Experimental Study","Inclusion Criteria:\n\n* Partially edentulous subjects between age group of 18 to 60 years.\n* Patients who require and are willing to receive a fixed dental prosthesis.\n* Patients with no experience of Fixed dental prosthesis previously.\n\nExclusion Criteria:\n\n* Patients diagnosed with any psychological disorders (diagnosed by physician).\n* Patients with facial anomalies like cleft lip and palate.\n* Patients with skeletal class 2 or class 3.\n* Patients with facial paralysis, stroke, and speech disorders.",{"count":102,"type":21},120,[24],"This study aims to assess patient satisfaction after receiving porcelain-fused-to-metal fixed dental prostheses. Patients will be asked about their expectations before treatment and their satisfaction afterward. The findings will help evaluate whether the treatment meets patient needs and guide improvements in dental care.",[106],"Patient Satisfaction",[108],"patient satisfaction PFM Prosthodontics","2025-08-02",{"date":111,"type":38},"2025-08-07",{"date":113,"type":21},"2025-10-01",{"date":115,"type":21},"2026-03-30",{"name":44,"class":45},""]