[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100496580":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":7,"centralContacts":8,"locations":14,"responsibleParty":50,"collaborators":52,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":58,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":7,"studyType":70,"phases":7,"briefSummary":71,"conditions":72,"keywords":75,"overallStatus":17,"whyStopped":7,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"1st SurgiConcept","INDUSTRY",null,[9],{"name":10,"role":11,"phone":12,"phoneExt":7,"email":13},"Dominique MALARD","CONTACT","+33 (0)320 23 41 96","dom@springthread.com",[15,30,37],{"facility":16,"status":17,"city":18,"state":7,"zip":7,"country":19,"countryCode":20,"cosmosGeoPoint":21,"geoPoint":26,"contacts":27},"Hôpital Henri Mondor","RECRUITING","Créteil","France","FR",{"type":22,"coordinates":23},"Point",[24,25],2.46569,48.79266,{"lat":25,"lon":24},[28],{"name":29,"role":11,"phone":7,"phoneExt":7,"email":7},"Barbara HERSANT, Pr",{"facility":16,"status":17,"city":18,"state":7,"zip":7,"country":19,"countryCode":20,"cosmosGeoPoint":31,"geoPoint":33,"contacts":34},{"type":22,"coordinates":32},[24,25],{"lat":25,"lon":24},[35],{"name":36,"role":11,"phone":7,"phoneExt":7,"email":7},"Jean-Paul MENINGAUD, Pr",{"facility":38,"status":39,"city":40,"state":7,"zip":41,"country":19,"countryCode":20,"cosmosGeoPoint":42,"geoPoint":46,"contacts":47},"Hôpital Pierre Paul Riquet","NOT_YET_RECRUITING","Toulouse","31000",{"type":22,"coordinates":43},[44,45],1.44367,43.60426,{"lat":45,"lon":44},[48],{"name":49,"role":11,"phone":7,"phoneExt":7,"email":7},"Céline DEKEISTER, Dr",{"type":51,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[53],{"name":54,"class":55},"EVAMED","OTHER","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":68,"type":69},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.",[73,74],"Ptosis","Ptosis, Mild",[76],"Ptosis, Moderate","2024-12-09",{"date":79,"type":80},"2024-12-12","ACTUAL",{"date":82,"type":80},"2023-02-16",{"date":84,"type":69},"2029-03",{"name":5,"class":6},3]