[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100565252":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":13,"centralContacts":17,"locations":25,"responsibleParty":47,"collaborators":7,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":58,"minAge":59,"maxAge":7,"enrollmentInfo":60,"targetDuration":7,"studyType":63,"phases":7,"briefSummary":64,"conditions":65,"keywords":70,"overallStatus":28,"whyStopped":7,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"University Hospital, Ghent","OTHER",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DIAGNOSTIC_TEST","Questionnaire","Questionnaire containing a combination of basic epidemiological questions, questions regarding recent sexual activity, questions regarding sexual preference and sexual activity, questions regarding the use of different types of erectile aids, questions regarding satisfaction with the use of these different erectile aid and questions regarding the satisfaction with sexual functioning and the partner relation. Al patients at least 6 months after primary genital gender-affirming surgery and who are sexually active are eligible.",[14],{"name":15,"affiliation":5,"role":16},"Anne-Françoise Spinoit, MD, PhD","PRINCIPAL_INVESTIGATOR",[18,23],{"name":19,"role":20,"phone":21,"phoneExt":7,"email":22},"Wietse Claeys, MD","CONTACT","003293322276","wietse.claeys@ugent.be",{"name":15,"role":20,"phone":21,"phoneExt":7,"email":24},"anne-francoise.spinoit@uzgent.be",[26],{"facility":27,"status":28,"city":29,"state":30,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"Department of Urology, University Hospital Ghent","RECRUITING","Ghent","East-Flanders","9000","Belgium","BE",{"type":35,"coordinates":36},"Point",[37,38],3.71667,51.05,{"lat":38,"lon":37},[41,42,43,44,45],{"name":19,"role":20,"phone":21,"phoneExt":7,"email":22},{"name":15,"role":20,"phone":21,"phoneExt":7,"email":24},{"name":15,"role":20,"phone":7,"phoneExt":7,"email":7},{"name":19,"role":20,"phone":7,"phoneExt":7,"email":7},{"name":46,"role":20,"phone":7,"phoneExt":7,"email":7},"Ina Brants, MA",{"type":48,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100565252","erectile-aid-use-in-post-phalloplasty-and-post-metoidioplasty-transgender-patients-100565252",false,"NCT06639763","Erectile Aid Use in Post-phalloplasty and Post-metoidioplasty Transgender Patients","Erectile Aid Use in Post-phalloplasty and Post-metoidioplasty Transgender Patients: an Epidemiological Survey","AID","Inclusion Criteria:\n\n* Patient and partner age ≥ 18 years.\n* Transgender or gender non-conforming individuals (and their partners).\n* Patients have undergone phalloplasty or metoidioplasty as a form of genital gender affirming surgery.\n* ≥6 months after phalloplasty or metoidioplasty (any type of flap or technique is allowed).\n* Sexually active or has been sexually active since phalloplasty or metoidioplasty with a partner or main sexual partner.\n* Voluntarily agreed that the data may be used for an anonymized scientific study.\n\nExclusion Criteria:\n\n* Patient age \\< 18 years.\n* Cisgender patients treated with phalloplasty or metoidioplasty for various reasons.\n* \\<6 months after phalloplasty or metoidioplasty.\n* Not sexually active since phalloplasty\u002Fmetoidioplasty.\n* Patient and\u002For partner have no interest in penetrative sexual intercourse.",true,"FEMALE","18 Years",{"count":61,"type":62},1000,"ESTIMATED","OBSERVATIONAL","This study seeks to explore the various methods used by transgender men for sexual intercourse following phalloplasty or metoidioplasty, focusing on their satisfaction with different erectile aids, as well as the satisfaction of their partners. Phalloplasty and metoidioplasty are gender-affirming surgeries that often require additional aids to achieve the desired sexual function, particularly for penetration. While internal erectile prostheses are common after phalloplasty, they come with high complication rates, leading some patients to opt for non-surgical aids. However, the effectiveness and comfort of these aids are not well-documented. This study aims to fill this gap by examining the types of aids transgender men use, how well these aids meet their sexual needs, and how satisfied both they and their partners are with the outcomes, providing much-needed insight for healthcare providers and patients alike.",[66,67,68,69],"Transgenderism","Erectile Dysfunction","Gender Dysphoria","Sexual Dysfunction",[71,72,73,74,75,76,77,78,79,80,81,82],"Gender dysphoria","Transgender","Phalloplasty","Metoidioplasty","Erectile dysfunction","Sexual function","Genital reconstruction","Reconstructive urology","Erectile aid","Patient Reported Outcome Measures (PROMs)","Erection prosthesis","Penile epithesis","2024-10-11",{"date":85,"type":86},"2024-10-15","ACTUAL",{"date":88,"type":86},"2024-07-06",{"date":90,"type":62},"2025-06-30",{"name":5,"class":6},1]