[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100617276":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":25,"locations":34,"responsibleParty":47,"collaborators":49,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":11,"eligibilityCriteria":58,"healthyVolunteers":54,"sex":59,"minAge":60,"maxAge":11,"enrollmentInfo":61,"targetDuration":11,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":74,"whyStopped":11,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"CMR Surgical Ltd","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Surgery with Versius","EXPERIMENTAL",null,[13],"Device: Versius Surgical System",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":11},"DEVICE","Versius Surgical System","Modular robotic system intended to assist in the accurate control of its surgical endoscopic instruments across a range of surgical procedures.",[9],[21],{"name":22,"affiliation":23,"role":24},"Bruno Domenico Antonio Alampi, MD","Division of General Oncologic and Minimally Invasive Surgery, Niguarda Hospital Milan","PRINCIPAL_INVESTIGATOR",[26,31],{"name":27,"role":28,"phone":29,"phoneExt":11,"email":30},"Mark Slack, MD","CONTACT","+44 7766 024389","mark.slack@cmrsurgical.com",{"name":32,"role":28,"phone":11,"phoneExt":11,"email":33},"Chad Schaber, PhD","chad.schaber@cmrsurgical.com",[35],{"facility":23,"status":11,"city":36,"state":11,"zip":11,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Milan","Italy","IT",{"type":40,"coordinates":41},"Point",[42,43],12.59836,42.78235,{"lat":43,"lon":42},[46],{"name":22,"role":24,"phone":11,"phoneExt":11,"email":11},{"type":48,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR",[50],{"name":23,"class":51},"UNKNOWN","100617276","versius-clinical-study-in-robot-assisted-inguinal-hernia-repair-surgery-100617276",false,"NCT07316517","Versius Clinical Study in Robot Assisted Inguinal Hernia Repair Surgery","Prospective Clinical Study to Evaluate the Safety and Efficacy of Versius in Robot-Assisted Inguinal Hernia Repair Surgery","Inclusion Criteria:\n\n1. Adult patients 22 years of age and older, deemed eligible for elective minimal invasive inguinal Hernia repair surgery.\n2. Patients providing written informed consent to participate in the study.\n\nExclusion Criteria:\n\n1. Patient unwilling to provide informed consent.\n2. Medical contraindication for general anaesthesia or minimally invasive procedure.\n3. Patient participation in an interventional clinical study that could impact primary outcomes results.\n4. Patient who falls into American Society of Anaesthesiologists (ASA) Class IV or above.\n5. Patients undergoing a concomitant surgical procedure.\n6. Contraindication for undergoing surgery with Versius (bleeding diathesis, active pregnancy or BMI ≥40 kg\u002Fm2).","ALL","22 Years",{"count":62,"type":63},30,"ESTIMATED","INTERVENTIONAL",[66],"NA","The objective of this clinical trial is to evaluate the safety and efficacy of Versius in Inguinal Hernia repair surgery",[69],"Robotic Assisted Inguinal Hernia Repair",[71,72,73],"Versius","Robotic surgery","Inguinal hernia","NOT_YET_RECRUITING","2025-12-18",{"date":77,"type":78},"2026-01-05","ACTUAL",{"date":80,"type":63},"2026-03",{"date":82,"type":63},"2026-12",{"name":5,"class":6},1]