[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100598764":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":34,"responsibleParty":50,"collaborators":10,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":10,"eligibilityCriteria":57,"healthyVolunteers":54,"sex":58,"minAge":59,"maxAge":10,"enrollmentInfo":60,"targetDuration":10,"studyType":63,"phases":10,"briefSummary":64,"conditions":65,"keywords":10,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"University of Minnesota","OTHER",[8,13,16],{"label":9,"type":10,"description":10,"interventionNames":11},"Standard of Care Cancer Screening",null,[12],"Other: No intervention",{"label":14,"type":10,"description":10,"interventionNames":15},"FDA approved self swab",[12],{"label":17,"type":10,"description":10,"interventionNames":18},"Mock self swab",[12],[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"No intervention","Observational study",[14,17,9],[25],{"name":26,"affiliation":5,"role":27},"Meredith Wise","PRINCIPAL_INVESTIGATOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":10,"email":33},"Maria Bunch","CONTACT","612-624-2018","obgynresearch@umn.edu",[35],{"facility":5,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"RECRUITING","Minneota","Minnesota","55455","United States","US",{"type":43,"coordinates":44},"Point",[45,46],-95.98559,44.55885,{"lat":46,"lon":45},[49],{"name":30,"role":31,"phone":32,"phoneExt":10,"email":33},{"type":51,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100598764","cervical-and-endometrial-cancer-screening-in-patients-seeking-gender-affirming-hysterectomy-100598764",false,"NCT07075731","Cervical and Endometrial Cancer Screening in Patients Seeking Gender-Affirming Hysterectomy","Inclusion Criteria:\n\n* 18 years and older\n* Able to provide voluntary written consent prior to the performance of any research related activity. Patients who can provide informed consent\n* Able to understand, speak, read, and write in English\n* Patients who have undergone hysterectomy, or plan to have a hysterectomy\n* Patients who are transgender and gender diverse\"\n\nExclusion Criteria:\n\n* Opted out of research\n* \\\u003C18 years old\n* Lacks capacity to consent\u002Fhas diminished capacity to consent\n* Cannot provide informed consent\n* Those on the study's community advisory board","ALL","18 Years",{"count":61,"type":62},40,"ESTIMATED","OBSERVATIONAL","This study aims to quantify the rates of cervical cancer screening and endometrial sampling prior to gender-affirming hysterectomy, assess the need for these tests in TGD individuals, and explore patient-centered options for these tests. By assessing the status of testing and correlation with hysterectomy pathology, this study will provide preliminary data on the current state of guideline-concordant care and provide initial evidence for the development of evidence-based guidelines in the future",[66,67,68],"Cancer Screening","Transgender","Gender Diverse Populations","2025-07-10",{"date":71,"type":72},"2025-07-20","ACTUAL",{"date":74,"type":72},"2025-06-30",{"date":76,"type":62},"2027-06-30",{"name":5,"class":6},1]