[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Botanee Group Co., Ltd.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":43},{"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":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100584636","a-clinical-study-on-pre-operative-intervention-with-products-during-aesthetic-medicine-100584636",false,"NCT06891924","A Clinical Study on Pre-operative Intervention With Products During Aesthetic Medicine","Clinical Study on Pre-operative Intervention With Products to Mitigate Skin Discomfort During Aesthetic Medicine","Inclusion Criteria:\n\n* health females aged 35-60;\n* subjects with rough dark, loose fine lines;\n* no history of cosmetic allergies;\n* subjects are willing to use the test serum on split-face for 28 days;\n* subjects are willing to suffer the Fotona 4D treatment (Frac3 and Piano modes) on the face;\n* subjects are willing to use the basic skincare products for 28 days, and acceptable for split-face use of the test products or the control product for 14 days;\n* written informed consent and portrait right consent were obtained from all participants before study entry.\n\nExclusion Criteria:\n\n* anyone who is pregnant, nursing an infant, or planning a pregnancy during the study;\n* subjects with known allergies or sensitivities to the ingredients in any of the study products;\n* any symptoms of facial flushing, erythema, papules, desquamation, or edema as evaluated by a physician prior to initial screening or Fotona4D Pro treatment;\n* unhealed skin lesions;\n* participated in any other clinical trial within one month;\n* received facial skin treatments including but not limited to lasers, chemical peels, and dermal fillers within one month;\n* taken\u002Finjected anti-allergy medication in the past one month;\n* participants in other clinical trials at the same time;\n* any subjects that the investigator considers ineligible.",true,"FEMALE","35 Years","60 Years",{"count":21,"type":22},33,"ESTIMATED","INTERVENTIONAL",[25],"NA","This clinical trial aims to evaluate whether a 14-day pre-operative application of the test product (containing MLYAAT-1002®, a proprietary anti-aging complex) can mitigate skin discomfort during Fotona 4D laser therapy (Frac3 and Piano modes) by comparing clinical evaluation, skin attributes measurement and subject self-assessment.",[28,29,30],"Skin Aging","Skin Condition","Skin Manifestations","NOT_YET_RECRUITING","2025-03-26",{"date":34,"type":35},"2025-04-01","ACTUAL",{"date":37,"type":22},"2025-03-25",{"date":39,"type":22},"2025-06-01",{"name":41,"class":42},"Botanee Group Co., Ltd.","INDUSTRY",""]