[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650433":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":10,"locations":10,"responsibleParty":18,"collaborators":10,"id":22,"slug":23,"hasResults":24,"nctId":25,"briefTitle":26,"officialTitle":27,"acronym":10,"eligibilityCriteria":28,"healthyVolunteers":29,"sex":30,"minAge":31,"maxAge":32,"enrollmentInfo":33,"targetDuration":10,"studyType":36,"phases":10,"briefSummary":37,"conditions":38,"keywords":10,"overallStatus":41,"whyStopped":10,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":10},{"fullName":5,"class":6},"Recep Tayyip Erdogan University Training and Research Hospital","OTHER",[8,12,15],{"label":9,"type":10,"description":11,"interventionNames":10},"Conventional Inferior Alveolar Nerve Block",null,"Participants in this cohort receive conventional inferior alveolar nerve block anesthesia as part of routine clinical care before vital pulp therapy of permanent mandibular first molars. The anesthesia technique is selected by the treating clinician according to standard clinical practice. No additional intervention or modification of the anesthesia procedure is performed for study purposes. Pain, dental anxiety, physiological parameters, and postoperative outcomes are evaluated and recorded.",{"label":13,"type":10,"description":14,"interventionNames":10},"QuickSleeper Computer-Controlled Local Anesthesia","Participants in this cohort receive computer-controlled local anesthetic delivery using the QuickSleeper system as part of routine clinical care before vital pulp therapy of permanent mandibular first molars. The anesthesia technique is selected by the treating clinician according to standard clinical practice. No additional intervention or modification of the routine treatment protocol is performed for study purposes. Pain, dental anxiety, physiological parameters, and postoperative outcomes are evaluated and recorded.",{"label":16,"type":10,"description":17,"interventionNames":10},"Controlled Local Anesthetic Delivery System Group","Participants in this cohort receive computer-controlled local anesthetic delivery using the SOAN system as part of routine clinical care before vital pulp therapy of permanent mandibular first molars. The SOAN system allows controlled administration of local anesthetic solution with regulated flow and pressure during the injection procedure. The anesthesia technique is selected by the treating clinician according to standard clinical practice and clinical requirements. No additional intervention, modification of the routine treatment protocol, or procedure solely for research purposes is performed. Dental anxiety, pain responses, physiological parameters, and postoperative outcomes are evaluated and recorded during and after the routine dental treatment process.",{"type":19,"investigatorFullName":20,"investigatorTitle":21,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","DİLARA NİL GÜNAÇAR","Assoc.Prof.","100650433","pain-and-anxiety-during-vital-pulp-therapy-using-different-local-anesthesia-techniques-in-children-100650433",false,"NCT07748390","Pain and Anxiety During Vital Pulp Therapy Using Different Local Anesthesia Techniques in Children","Evaluation of the Effects of Different Local Anesthesia Techniques on Dental Anxiety and Pain During Vital Pulp Therapy","Inclusion Criteria:\n\n* Children aged 8-10 years.\n* Children and parents\u002Flegal guardians who agree to participate in the study and provide informed consent.\n* Patients requiring vital pulp therapy of a permanent mandibular first molar.\n* Patients classified as Frankl Behavior Rating Scale score 3 or 4. Systemically healthy children (ASA I).\n* Children with adequate cognitive and communication abilities to understand the study procedures and pain\u002Fanxiety assessment scales.\n* Permanent mandibular first molars without clinical or radiographic signs of abscess, fistula, or periapical pathology.\n\nExclusion Criteria:\n\n* Children with systemic diseases or medical conditions affecting dental treatment.\n* Children classified as Frankl Behavior Rating Scale score 1 or 2.\n* Patients with known allergy or hypersensitivity to local anesthetic agents (e.g., lidocaine, articaine).\n* Teeth with acute dental infection signs, including abscess, cellulitis, or extensive infection.\n* Teeth showing clinical or radiographic evidence of periapical pathology.\n* Children unable to understand or complete pain and anxiety assessment scales due to cognitive, visual, hearing, or communication limitations.\n* Patients who do not comply with the study procedures or withdraw consent.",true,"ALL","8 Years","10 Years",{"count":34,"type":35},120,"ESTIMATED","OBSERVATIONAL","This prospective observational study aims to evaluate the effects of different local anesthesia techniques on dental anxiety and pain in children undergoing vital pulp therapy of permanent mandibular first molars. Conventional inferior alveolar nerve block and two computer-controlled local anesthetic delivery (CCLAD) systems used in routine clinical practice will be compared. The choice of anesthesia technique will be based on the clinician's routine decision-making, and no additional intervention or modification of standard treatment will be performed for research purposes. Dental anxiety, pain, physiological parameters, and postoperative complications will be assessed using validated clinical scales and routine clinical measurements. The findings may help improve pain and anxiety management during pediatric dental treatment while supporting evidence-based selection of local anesthesia techniques.",[39,40],"Pediatric","Anesthesia","NOT_YET_RECRUITING","2026-07-31",{"date":44,"type":45},"2026-08-05","ACTUAL",{"date":47,"type":35},"2026-08-01",{"date":49,"type":35},"2026-12-30",{"name":5,"class":6}]