[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cutis-laxa\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cutis-laxa":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"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":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100641497","effectiveness-and-safety-of-the-ulthera-system-for-skin-laxity-in-the-lower-face-submentum-and-neck-100641497",false,"NCT07614997","Effectiveness and Safety of the Ulthera® System for Skin Laxity in the Lower Face, Submentum and Neck","Evaluation of the Effectiveness and Safety of the Ulthera® System for Treating Skin Laxity in the Lower Face, Submentum and Neck","Inclusion Criteria:\n\n* Mild to moderate lower face, submental and\u002For neck laxity, that is amenable to improvement with non-invasive intervention and not severe enough for surgical intervention.\n* Willing to abstain from all other aesthetic treatments on ANY part of the face, submentum or neck, including but not limited to injectable fillers, implants, neurotoxin, skin peels, laser treatments, surgical treatments, etc. for the clinical investigation's duration.\n* Willing and able to refrain from chronic use of aspirin, ibuprofen, naproxen, or other nonsteroidal anti-inflammatory drugs (NSAIDs) for 10 to 14 days post-treatment.\n* Has an adequate understanding of the Chinese language.\n* Willing and able to comply with protocol requirements.\n\nExclusion Criteria:\n\n* Scarring in area(s) to be treated.\n* Any active implants.\n* Any metallic implants in area(s) to be treated.\n* Any open wounds or lesions, including active herpes simplex, in the area(s) to be treated.\n* Presence of an active systemic or local skin disease, including active, cystic, or severe inflammatory acne in the area(s) to be treated.\n* History of keloid formation or hypertrophic scarring.\n* History of the following cosmetic treatments in area(s) to be treated:\n\n  * Skin-tightening procedure,\n  * Injectable crosslinked hyaluronic acid (HA)\u002Fcollagen temporary dermal fillers of the lower face, submentum or neck within the past 12 months.\n  * Injectable non-crosslinked HA dermal fillers of the lower face, submentum or neck within the past 6 months.\n  * Injectable semi-permanent\u002Fpermanent facial fillers\n  * Neurotoxin treatment of the lower face, submentum or neck within the past 6 months.\n  * Liposuction of the lower face, submentum or neck within the last 12 months.\n  * Fat grafting of the lower face, submentum or neck within the last 12 months.\n  * Deoxycholic acid within the last 12 months; and\u002For\n  * Chemical peeling or dermabrasion treatments within the past 12 months.\n  * Cryolipolysis\n* Had prior surgery in the lower-facial area and\u002For neck\u002Fsubmentum or has a permanent implant or graft in the lower-facial area that could interfere with effectiveness assessments.\n* Has undergone oral surgery in the past 30 days.\n* Participants who have used isotretinoin or other retinoid medications within 6 months prior to enrollment or have applied topical retinoid-containing medications on the face or neck area within 2 weeks prior to enrollment or planning such treatments during the study period.\n* Marked facial asymmetry, deep dermal scarring, or thick sebaceous skin in the full face.\n* Severe solar elastosis.\n* Facial nerve palsy or history of facial nerve palsy.\n* Tattoos in the area(s) to be treated (excluding microblading eyebrow).\n* Current smoker or history of smoking in the last 12 months.\n* Current daily user of any nicotine-containing products\n* Is a female of childbearing potential1 and not using medically effective birth control 2 or is pregnant, lactating, or planning to become pregnant during the clinical investigation.",true,"ALL","35 Years","65 Years",{"count":21,"type":22},218,"ESTIMATED","INTERVENTIONAL",[25],"NA","The purpose of this study is to demonstrate superiority of treatment with the Ulthera System compared to untreated control for the improvement of skin laxity of the lower face, submental area and neck and to demonstrate the safety of treatment with the Ulthera System for the improvement of skin laxity of the lower face, submental area and neck.",[28],"Cutis Laxa",[30],"Skin laxity","RECRUITING","2026-06-16",{"date":34,"type":35},"2026-06-17","ACTUAL",{"date":37,"type":35},"2026-06-15",{"date":39,"type":22},"2027-03",{"name":41,"class":42},"Merz North America, Inc.","INDUSTRY",7,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":75},"100541475","qualitative-study-in-patients-with-genodermatoses-and-healthcare-professionals-on-reproductive-counselling-100541475","NCT06330350","Qualitative Study in Patients With Genodermatoses and Healthcare Professionals on Reproductive Counselling","Investigating Perspectives of Patients With Genodermatosis and Healthcare Professionals on Reproductive Counselling","Inclusion Criteria:\n\n* Adult patients with genodermatosis (i.e, keratinisation disorders, skin fragility diseases, ectodermal dysplasias, dermato-oncological syndromes, other genodermatoses) and a desire to have children, with if applicable his or her partner with a desire to have children\n* Patients with clinically and molecularly confirmed variant of a genodermatosis\n* Health care professionals involved with the care of genodermatology patients (e.g. clinical geneticists, dermatologists)\n\nExclusion Criteria:\n\n* Not being able to communicate verbally in Dutch or English",{"count":52,"type":22},25,"OBSERVATIONAL","The goal of this observational study is to understand the perspectives and needs of patients with genodermatoses and their partners who wish to have children, regarding their decision-making process and their consideration of reproductive options. Additionally, the investigators aim to investigate the level of knowledge and perspectives of healthcare professionals (such as clinical geneticists, dermatologists and other clinicians involved), and want to explore to what extent patients and their partners are well informed about these reproductive options. To achieve this, the investigators will conduct individual semi-structured qualitative interviews with participants affected by genodermatoses (and their partners) and with healthcare professionals.",[56,57,58,59,60,61,62,63,28,64],"Quality of Life","Ichthyosis","Palmoplantar Keratoses","Epidermolysis Bullosa","Ectodermal Dysplasia","Basal Cell Nevus Syndrome","Birt-Hogg-Dube Syndrome","Tuberous Sclerosis","Albinism","2025-05-16",{"date":67,"type":35},"2025-05-18",{"date":69,"type":35},"2024-01-01",{"date":71,"type":22},"2025-12-31",{"name":73,"class":74},"Maastricht University Medical Center","OTHER",1]