[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abnormal-labial-frenum-frenectomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abnormal-labial-frenum-frenectomy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":48,"leadSponsor":50,"locationsCount":5},"100647205","pain-after-diode-laser-frenectomy-in-children-100647205",false,"NCT07706023","Pain After Diode Laser Frenectomy in Children","Postoperative Pain Assessment Following Diode Laser-Assisted Frenectomy in Pediatric Patients: A Prospective Single-Group Clinical Study","PED-FREN","Inclusion Criteria:\n\n* Children aged 8 to 14 years.\n* Patients requiring diode laser-assisted frenectomy based on clinical indication.\n* American Society of Anesthesiologists (ASA) Physical Status I or II.\n* Ability of the participant and parent\u002Flegal guardian to understand the study procedures.\n* Written informed consent obtained from the parent or legal guardian, with assent obtained from the child when appropriate.\n\nExclusion Criteria:\n\n* Presence of systemic diseases or medical conditions that could influence wound healing or pain perception.\n* Current use of analgesic, anti-inflammatory, corticosteroid, or psychotropic medications.\n* History of allergy or contraindication to local anesthetic agents.\n* Acute oral infection at the surgical site.\n* Previous oral soft tissue surgery in the same anatomical region.\n* Inability or unwillingness to complete the postoperative pain assessment forms for seven consecutive days.\n* Withdrawal of consent at any time during the study.",true,"ALL","8 Years","14 Years",{"count":22,"type":23},53,"ESTIMATED","INTERVENTIONAL",[26],"NA","This prospective single-group clinical study aims to evaluate postoperative pain following diode laser-assisted frenectomy in pediatric patients and to assess the agreement between different pediatric pain assessment scales. Children aged 8 to 14 years who require diode laser-assisted frenectomy will be treated according to the standard clinical protocol at the Pediatric Dentistry Clinic of Afyonkarahisar Health Sciences University. Postoperative pain will be evaluated once daily for seven consecutive days using the Wong-Baker FACES Pain Rating Scale, the Modified Emoji Pain Scale (MEPS), and gender-specific pain assessment scales. The primary objective is to characterize the time course of postoperative pain during the first postoperative week. Secondary objectives include evaluating the agreement and correlation between the different pain assessment instruments used in pediatric patients. The findings are expected to contribute to the identification of reliable pain assessment methods and to improve postoperative pain evaluation following diode laser-assisted frenectomy in children.",[29,30],"Abnormal Labial Frenum Frenectomy","Frenectomy",[32,33,34,35,36,37,38,39,40,41],"Diode Laser","Laser Frenectomy","Pediatric Dentistry","Postoperative Pain","Pain Assessment","Wong-Baker FACES Pain Rating Scale","Modified Emoji Pain Scale","Children","Oral Surgery","Frenulum Abnormalities","NOT_YET_RECRUITING","2026-07-10",{"date":45,"type":46},"2026-07-15","ACTUAL",{"date":43,"type":23},{"date":49,"type":23},"2026-12-31",{"name":51,"class":52},"Afyonkarahisar Health Sciences University","OTHER"]