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