[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"prolapse-vaginal\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:prolapse-vaginal":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,72],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100598463","transperineal-ultrasound-evaluation-of-vesicourethral-angle-and-de-novo-sui-after-colpocleisis-surgery-100598463",false,"NCT07071818","Transperineal Ultrasound Evaluation of Vesicourethral Angle and de Novo SUI After Colpocleisis Surgery","Evaluation of the Vesicourethral Angle by Preoperative and Postoperative Transperineal Ultrasound in Patients Undergoing Colpocleisis Surgery and Assessment of de Novo Urinary Incontinence","colpocleisis","Inclusion Criteria:\n\nPostmenopausal women with stage 3 or 4 pelvic organ prolapse (according to POP-Q score), who are not sexually active and do not desire future vaginal intercourse, and who consent to undergo colpocleisis surgery will be included in the study.\n\nExclusion Criteria:\n\nThose with a history of stress incontinence surgery Those who underwent an additional vesicourethral intervention in addition to colpocleisis surgery Those who wanted sexual intercourse","FEMALE","60 Years","75 Years",{"count":21,"type":22},31,"ESTIMATED","INTERVENTIONAL",[25],"NA","This prospective observational study aims to evaluate changes in the vesicourethral angle using transperineal ultrasound before and after colpocleisis surgery, and to assess the relationship of these changes with the development of de novo stress urinary incontinence.",[28],"Prolapse, Vaginal",[30,31,32,33],"Colpocleisis","Transperineal Ultrasound","de Novo Incontinence","Vesicourethral Angle","RECRUITING","2025-07-15",{"date":37,"type":38},"2025-07-17","ACTUAL",{"date":40,"type":38},"2025-07-01",{"date":42,"type":22},"2026-01-01",{"name":44,"class":45},"Gaziosmanpasa Research and Education Hospital","OTHER_GOV",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":46},"100598142","post-hysterectomy-vaginal-length-horizontal-vs-vertical-closure-100598142","NCT07067645","Post-Hysterectomy Vaginal Length: Horizontal vs. Vertical Closure","Investigation of the Effect of Horizontal and Vertical Vaginal Cuff Closure on Postoperative Total Vaginal Length in Patients Undergoing Vaginal Hysterectomy and Lateral Suspension","vagina","Inclusion Criteria:\n\n* Cases with vaginal hysterectomy and lateral suspension surgery due to stage 3-4 uterine prolapse Agree to participate in the study and sign the informed consent form\n\nExclusion Criteria:\n\n* Cases that have previously undergone a different suspension surgery due to descent uteri (vaginal hysterectomy and sacrospinous ligament fixation surgery, vaginal hysterectomy and sacrocolopexy surgery, vaginal hysterectomy and high sacouterin plication surgery) Cases that have undergone vaginal hysterectomy due to malignancy Cases that have undergone radiotherapy due to malignancy (brachytherapy) Patients who are not suitable for surgical intervention due to severe vaginal atrophy.\n\nPatients who will not be able to comply with the follow-up process. Not accepting to participate in the study or not signing the informed consent form","35 Years","65 Years",{"count":58,"type":22},62,[25],"This prospective clinical study aims to evaluate the impact of vaginal cuff closure orientation-horizontal versus vertical-on postoperative total vaginal length in patients undergoing vaginal hysterectomy combined with lateral suspension. By comparing anatomical outcomes between the two closure techniques, the study seeks to determine which method better preserves vaginal length, potentially influencing surgical preferences and postoperative quality of life.",[28,62],"Vaginal Vault Prolapse",[64,65],"Vault suspension","vaginal length",{"date":67,"type":38},"2025-07-16",{"date":40,"type":38},{"date":70,"type":22},"2026-03-01",{"name":44,"class":45},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":17,"minAge":79,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":23,"phases":82,"briefSummary":83,"conditions":84,"keywords":85,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":99},"100352985","vaginal-native-tissues-repair-for-pelvic-organ-prolapse-100352985","NCT03875989","Vaginal Native Tissues Repair for Pelvic Organ Prolapse","TAPP","Inclusion Criteria:\n\n* Patient at 50 years of age or older\n* Symptomatic primary prolapse of the anterior vaginal wall defined by Aa and\u002For Ba points ≥0 according to the POP-Q system\n* A positive response to the question \"Do you usually have a bulge or something falling out that you can see or feel in your vaginal area?\" (question 3 of the PFDI-20)\n* Able to give informed consent\n* Performans Status score ≤ 2\n\nExclusion Criteria:\n\n* Patient with need for surgical treatment for myorraphy of levator ani muscles\n* Patient with previous surgical cystocele repair.\n* Patient with evolving gynaecologic cancer.\n* Pregnancy or wish for future pregnancy, lactating woman.\n* Inability to participate in study follow-up or to provide informed consent.\n* Lack of social insurance .","50 Years",{"count":81,"type":22},214,[25],"The aim of the study is to assess at one year the effectiveness of the vaginal patch plastron in comparison of the anterior colporraphy through a combined definition of success: anatomic and functional.",[28],[86,87,88],"Prolapse","Vaginal native tissues repair","Pelvic organ","2023-08-28",{"date":91,"type":38},"2023-08-29",{"date":93,"type":38},"2019-09-27",{"date":95,"type":22},"2028-03-27",{"name":97,"class":98},"University Hospital, Limoges","OTHER",9]