[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Distalmotion SA\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":83},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,61],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100650499","robotic-minimally-invasive-benign-hysterectomy-post-market-clinical-study-with-the-dexter-robotic-system-100650499",false,"NCT07746531","Robotic Minimally Invasive Benign Hysterectomy Post-market Clinical Study With the DEXTER Robotic System","ROBOTIC MINIMALLY INVASIVE HYSTERECTOMY POST-MARKET CLINICAL STUDY WITH THE DEXTER ROBOTIC SURGERY SYSTEM","MAGENTA","Inclusion Criteria:\n\n* Patient is ≥ 22 years of age at time of enrollment\u002Fconsent\n* Patient is planned to undergo robotic-assisted and laparoscopic hysterectomy for benign disease\n* Patient agrees to perform the 6-week follow-up assessment as per standard of care\n\nExclusion Criteria:\n\n* Any planned concomitant procedures (not including salpingectomy and\u002For oophorectomy)\n* Diagnosed malignant disease on reproductive organs\n* Uterus myomatous with fibroid \\> 10cm","FEMALE","22 Years",{"count":20,"type":21},112,"ESTIMATED","OBSERVATIONAL","The purpose of this post-market, observational study is to collect real-world data under anticipated conditions of use that demonstrates that the device performs as intended (accurate, precise control of surgical instruments) in patients undergoing robotic-assisted and laparoscopic hysterectomy for benign disease.",[25],"Hysterectomy, Benign Uterine Diseases","NOT_YET_RECRUITING","2026-07-31",{"date":29,"type":30},"2026-08-05","ACTUAL",{"date":32,"type":21},"2026-08-07",{"date":34,"type":21},"2028-12",{"name":36,"class":37},"Distalmotion SA","INDUSTRY",2,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":46,"minAge":18,"maxAge":4,"enrollmentInfo":47,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":49,"conditions":50,"keywords":4,"overallStatus":52,"whyStopped":4,"lastUpdateSubmitDate":53,"lastUpdatePostDateStruct":54,"startDateStruct":56,"completionDateStruct":58,"leadSponsor":60,"locationsCount":38},"100606924","robotic-minimally-invasive-inguinal-hernia-repair-post-market-clinical-study-with-the-dexter-robotic-system-100606924","NCT07181876","Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System","RAS-ACCESS","Inclusion Criteria:\n\n* Subject is ≥ 22 years of age at time of enrollment\u002Fconsent\n* Subject is indicated for and planned to undergo robot-assisted and laparoscopic surgery for unilateral or bilateral inguinal hernia repair\n* Subject is able and willing to comply with the protocol requirements, has been informed of the nature of the study, and has signed the IRB-approved informed consent form\n\nExclusion Criteria:\n\n* Subject with any relative and absolute contraindications for the use of conventional endoscopes and endoscopic surgical instruments and\u002For general non-procedure specific contraindications to endoscopic surgery including bleeding diathesis and pregnancy\n* Subject is participating in another clinical investigation at the time of enrollment or planned participation at any time during this clinical study\n* Subject has a known or suspected medical condition that, in the opinion of the Investigator, may put the subject at risk for participation in this clinical study","ALL",{"count":48,"type":21},140,"The purpose of this post-market, observational study is to collect data under anticipated conditions of use that demonstrates that DEXTER performs as intended in the intended patient population, including a variety of representative disease etiologies and demographic groups.",[51],"Inguinal Hernia Repair","RECRUITING","2026-07-02",{"date":55,"type":30},"2026-07-06",{"date":57,"type":30},"2025-11-26",{"date":59,"type":21},"2029-12",{"name":36,"class":37},{"id":62,"slug":63,"hasResults":11,"nctId":64,"briefTitle":65,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":11,"sex":46,"minAge":68,"maxAge":4,"enrollmentInfo":69,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":71,"conditions":72,"keywords":4,"overallStatus":52,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},"100602403","robotic-assisted-right-colectomy-with-the-dexter-robotic-surgery-system-100602403","NCT07123051","Robotic Assisted Right Colectomy With the DEXTER Robotic Surgery System","RACER","Inclusion Criteria:\n\n* Aged \\> 18 years\n* Patient agrees to perform the 30-day follow-up assessment as per standard of care\n\nExclusion Criteria:\n\n* History of radiotherapy on the target surgical area\n* Patients with distant metastasis\n* Any planned concomitant procedures\n* History of major abdominal surgery","18 Years",{"count":70,"type":21},33,"This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing robotic-assisted right colectomy.",[73],"Right Colectomy","2026-04-10",{"date":76,"type":30},"2026-04-13",{"date":78,"type":30},"2025-08-05",{"date":80,"type":21},"2026-09",{"name":36,"class":37},4,""]