[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"1st SurgiConcept\",\"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":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100496580","performance-and-safety-assessment-of-spring-thread-elastic-tensor-thread-in-patients-with-mild-to-moderate-facial-ptosis-100496580",false,"NCT05746078","Performance and Safety Assessment of SPRING THREAD® Elastic Tensor Thread in Patients with Mild to Moderate Facial Ptosis.","Long-term Assessment of the Performance and Safety of SPRING THREAD® Elastic Tensor Thread.","ESTES","Inclusion Criteria:\n\n* Men \u002F women aged 35 to 75 with facial ptosis (cheekbones, jowls) with or without a history of aesthetic treatment (botox, filler, surgical lift).\n* Patient able to understand the explanations given.\n* Patient informed and not objecting to participate in the study.\n* Patient able to comply with protocol requirements, including follow-up visits.\n* Patient affiliated to social security.\n\nExclusion Criteria:\n\n* Patient unable to understand study information and attend study visits.\n* Patient did not give consent to participate.\n* Patients who have had a previous facial rejuvenation treatment in the 3 months prior to the study.\n* Patients treated with long-term systemic corticosteroids.\n* Patients with visceral failure, chronic immunological pathology, pregnant or breasfeading women.\n* Patient participating or having participated in another clinical trial protocol, drug or medical device within 30 days of inclusion.\n* Patient refusing to participate in the clinical investigation.","ALL","35 Years","75 Years",{"count":21,"type":22},99,"ESTIMATED","OBSERVATIONAL","The purpose of this post-market clinical follow up study is to assess the safety and effectiveness of the SPRING THREAD® elastic tensor thread. The study will evaluate the outcome of the SPRING THREAD® elastic tensor thread range over a period of 5 years.",[26,27],"Ptosis","Ptosis, Mild",[29],"Ptosis, Moderate","RECRUITING","2024-12-09",{"date":33,"type":34},"2024-12-12","ACTUAL",{"date":36,"type":34},"2023-02-16",{"date":38,"type":22},"2029-03",{"name":40,"class":41},"1st SurgiConcept","INDUSTRY",3,""]