[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tinea-capitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tinea-capitis":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100607103","comparison-between-continuous-and-pulse-itraconazole-in-tinea-capitis-in-children-100607103",false,"NCT07184203","Comparison Between Continuous and Pulse Itraconazole in Tinea Capitis in Children","Comparative Clinicomycologic and Dermoscopic Study Between Daily and Pulse Therapy of Oral Itraconazole in Tinea Capitis in Children","Inclusion Criteria:\n\n• Tinea capitis patients with ages ranging from 5 to 18 year\n\nExclusion Criteria:\n\n* Patients with contraindications to itraconazole\n* Patients with associated scalp disease.\n* Patients weighing less than 20 Kg.","ALL","5 Years","18 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24],"NA","A study to compare the efficacy of daily therapy versus pulse therapy of oral itraconazole in the treatment of tinea capitis in children based on clinical, mycological and dermoscopic evaluation.",[27],"Tinea Capitis","RECRUITING","2025-09-14",{"date":31,"type":32},"2025-09-19","ACTUAL",{"date":34,"type":32},"2025-03-09",{"date":36,"type":21},"2025-12-31",{"name":38,"class":39},"Alexandria University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":18,"enrollmentInfo":48,"targetDuration":50,"studyType":51,"phases":4,"briefSummary":52,"conditions":53,"keywords":54,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":40},"100596555","population-pharmacokinetics-of-terbinafine-in-children-with-tinea-capitis-100596555","NCT07046988","Population Pharmacokinetics of Terbinafine in Children With Tinea Capitis","Inclusion Criteria:\n\n1. Aged 2 to 18 years;\n2. Diagnosis of tinea capitis:\n\n   * Typical clinical manifestations, dermatoscopic findings combined with Wood's lamp examination; ② Positive mycological examination, including positive fungal microscopy and\u002For isolation of dermatophytes by fungal culture; ③ Exclusion of scalp seborrheic dermatitis, psoriasis, alopecia areata, lupus erythematosus, lichen planopilaris, trichotillomania, suppurative perifolliculitis of scalp, syphilitic alopecia, etc.\n\nExclusion Criteria:\n\n1. Concomitant topical treatment with terbinafine;\n2. Conditions interfering with gastrointestinal absorption of terbinafine;\n3. Documented hepatic\u002Frenal impairment or hematological disorders;\n4. Receipt of radiotherapy, systemic cytostatic\u002Fimmunosuppressive therapy, or antibacterial\u002Fantiviral\u002Fantiparasitic therapy currently or within 2 weeks prior to study initiation;\n5. Participation in other clinical trials, or other circumstances deemed inappropriate by the investigator.","2 Years",{"count":49,"type":21},60,"4 Weeks","OBSERVATIONAL","The goal of this observational study is to characterize the population pharmacokinetics (PPK) of terbinafine in pediatric patients with tinea capitis, evaluate its efficacy and safety, and identify covariates affecting drug disposition in Chinese children aged 2-18 years diagnosed with tinea capitis and treated with oral terbinafine. The main questions it aims to answer are:\n\nWhat are the terbinafine pharmacokinetic parameters (e.g., AUC, CL, V) in children with tinea capitis, and how do they differ from adult values? Which covariates (e.g., age, body weight, CYP enzyme activity, renal function) significantly influence inter-individual variability in terbinafine PK parameters? What is the clinical efficacy (based on TSSS reduction and mycological cure rate) and safety profile of terbinafine in this pediatric population?\n\nParticipants will:\n\nUndergo oral terbinafine treatment according to weight-based dosing (62.5-250 mg daily).\n\nConcentration determination is carried out using the opportunistic sampling method.\n\nComplete clinical assessments (TSSS scoring) and mycological examinations (microscopy\u002Fculture) at baseline and follow-up visits.\n\nUndergo routine laboratory tests (liver\u002Fkidney function, hematology) to monitor safety.",[27],[27],"2025-06-30",{"date":57,"type":32},"2025-07-02",{"date":59,"type":32},"2021-06-15",{"date":61,"type":21},"2026-06-01",{"name":63,"class":39},"Shandong University"]