[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100490918":3},{"organization":4,"outcomesModule":7,"designInfo":17,"detailedDescription":23,"studyPopulation":16,"armGroups":24,"interventions":31,"overallOfficials":41,"centralContacts":16,"locations":45,"responsibleParty":67,"collaborators":69,"id":73,"slug":74,"hasResults":75,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":16,"eligibilityCriteria":79,"healthyVolunteers":75,"sex":80,"minAge":81,"maxAge":16,"enrollmentInfo":82,"targetDuration":16,"studyType":85,"phases":86,"briefSummary":88,"conditions":89,"keywords":16,"overallStatus":48,"whyStopped":16,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"City of Hope Medical Center","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":16,"otherOutcomes":16},[9,13],{"measure":10,"description":11,"timeFrame":12},"Conversion of operation to laparotomy","The number and frequency will be reported with 95% confidence intervals.","Within 30 days of operation",{"measure":14,"description":15,"timeFrame":12},"Incidence of major surgical complications","Will be assessed by Clavien-Dindo classification as grade 3 or higher. The number and frequency will be reported with 95% confidence intervals.",null,{"allocation":18,"interventionModel":19,"interventionModelDescription":16,"primaryPurpose":20,"observationalModel":16,"timePerspective":16,"maskingInfo":21},"NA","SINGLE_GROUP","DEVICE_FEASIBILITY",{"masking":22,"maskingDescription":16,"whoMasked":16},"NONE","PRIMARY OBJECTIVE:\n\nI. To evaluate the effectiveness and safety for abdominal and pelvic procedures of a single-port robotic device (da Vinci SP1098) that is Food and Drug Administration (FDA)-approved for other indications, specifically urological and transoral otolaryngology surgical procedures.\n\nOUTLINE:\n\nPatients undergo surgery using the da Vinci SP1098 robotic system on study.",[25],{"label":26,"type":27,"description":28,"interventionNames":29},"Device feasibility (da Vinci SP1098 robotic system)","EXPERIMENTAL","Patients undergo surgery using the da Vinci SP1098 robotic system on study.",[30],"Device: Robot-Assisted Surgery",[32],{"type":33,"name":34,"description":35,"armGroupLabels":36,"otherNames":37},"DEVICE","Robot-Assisted Surgery","Undergo surgery using the da Vinci SP device",[26],[38,39,40],"Navigation and Robotics","Robot Assisted","Robotic Surgery",[42],{"name":43,"affiliation":5,"role":44},"Mehdi Moslemi-Kebria","PRINCIPAL_INVESTIGATOR",[46],{"facility":47,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"City of Hope Comprehensive Cancer Center","RECRUITING","Duarte","California","91010","United States","US",{"type":55,"coordinates":56},"Point",[57,58],-117.97729,34.13945,{"lat":58,"lon":57},[61,66],{"name":62,"role":63,"phone":64,"phoneExt":16,"email":65},"Mehdi Moslemi-kebria","CONTACT","909-949-2242","mkebria@COH.org",{"name":62,"role":44,"phone":16,"phoneExt":16,"email":16},{"type":68,"investigatorFullName":16,"investigatorTitle":16,"investigatorAffiliation":16,"oldNameTitle":16,"oldOrganization":16},"SPONSOR",[70],{"name":71,"class":72},"National Cancer Institute (NCI)","NIH","100490918","phase-2-the-da-vinci-single-port-robotic-system-for-use-in-abdominal-and-pelvic-surgical-procedures-100490918",false,"NCT05672368","The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures","Phase II Study of the Da Vinci Single Port (SP) Robotic System for Abdominal and Pelvic Procedures","Inclusion Criteria:\n\n* Documented informed consent of the participant and\u002For legally authorized representative\n* Any patient scheduled to undergo robot-assisted abdominal or pelvic procedures\n* Age \\> 18 years\n\nExclusion Criteria:\n\n* Body mass index (BMI) \\> 45\n* Contraindications to minimally invasive surgery including chronic obstructive pulmonary disorders\n* Past history of failed attempt of minimally invasive abdominal or pelvic surgery","ALL","18 Years",{"count":83,"type":84},33,"ESTIMATED","INTERVENTIONAL",[87],"PHASE2","This phase II trial test the effectiveness and safety of a single-port robotic device (the da Vinci single port \\[SP\\]1098) for use in abdominal and pelvic surgeries. The da Vinci SP1098 robotic device can be used to perform less invasive surgeries that allow entry into the body through a single, small incision. The use of this device during surgery may allow surgeons to perform complex procedures that result in less pain, fewer complications and side effects, and improved recovery.",[90],"Disease or Disorder","2026-10-05",{"date":93,"type":94},"2026-10-08","ACTUAL",{"date":96,"type":94},"2024-04-26",{"date":98,"type":84},"2027-09-21",{"name":5,"class":6},1]