[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"genital-prolapse\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:genital-prolapse":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,72],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100616523","laparoscopic-pectopexy-with-and-without-mesh-use-for-pelvic-organ-prolapse-100616523",false,"NCT07306715","Laparoscopic Pectopexy With and Without Mesh Use for Pelvic Organ Prolapse.","Comparison of Pectopexy Operations With and Without Mesh Use After Laparoscopic Hysterectomy for Pelvic Organ Prolapse.","Inclusion Criteria:\n\n* Female patients older than 40 years and younger than 80 years old with symptomatic uterine prolapse\n* Patients who provided written consent for the surgical procedure\n* Patients who do not wish to preserve their uterus\n\nExclusion Criteria:\n\n* Patients who cannot obtain anesthesia approval for laparoscopic surgery\n* Patients who have a confirmed or suspected pregnancy\n* Patients who have abnormal uterine\u002Fcervical\u002Fvaginal bleeding\n* Patients with biopsy-confirmed endometrial hyperplasia or cervical dysplasia\n* Patients with pathology-confirmed genital cancer\n* Patients undergone chemotherapy or radiotherapy for any type of cancer","FEMALE","40 Years","80 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","Genital apical prolapse refers to the descent of the vaginal apex, uterus, or cervix, and surgical treatment is required for adequate apical support. Laparoscopic pectopexy is a surgical method developed as an alternative to the gold standard, sacrocolpopexy, in the treatment of genital organ prolapse, especially for obese patients for whom dissection is difficult. The vaginal cuff is attached to the pectineal ligament with polypropylene mesh in the standard technique. The use of mesh is subject to serious restrictions due to complications such as mesh erosion. Surgical methods without using a mesh may be safer treatment options for patients with genital prolapse. This study aimed to compare the results of Laparoscopic Pectopexy surgery with and without the use of mesh material after hysterectomy.",[27],"Genital Prolapse",[29,30],"pectopexy","mesh","RECRUITING","2026-01-29",{"date":34,"type":35},"2026-02-02","ACTUAL",{"date":32,"type":35},{"date":38,"type":21},"2027-06-01",{"name":40,"class":41},"Kocaeli University","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":59,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":71},"100598074","safety-and-performance-of-a-pelvic-floor-mesh-implant-latgynious-100598074","NCT07066761","Safety and Performance of a Pelvic Floor Mesh Implant (LatGYNious)","Safety and Performance of a Pelvic Floor Mesh Implant for Laparoscopic Lateral Suspension (LatGYNious)","Inclusion Criteria:\n\n* Symptomatic prolapse in one of the 3 compartments from grade 2 with or without uterus\n* Subject is candidate for a surgical treatment of pelvic organ prolapse\n* Subject is willing and able to cooperate with follow-up examinations\n* Subject has been informed of the study procedures and the treatment and has signed an informed consent form and provided authorization to use and disclose information for research purposes.\n\nExclusion Criteria:\n\n* Previous surgical treatment with a mesh implant for pelvic organ prolapse (mesh implant in anterior or posterior compartment)\n* Active immunotherapy which may negatively affect the treatment with a surgical mesh\n* Active cancer of the vagina \u002F cervix \u002F rectum\n* . known or suspected hypersensitivity to Polypropylene\n* Pregnancy\n* participation in another study at the same time\n* Unable to understand study requirements or is unable to comply with follow-up schedule\n* Contraindicated according to the instruction for use of the device","18 Years",{"count":52,"type":21},85,[24],"The purpose of the clinical investigation is to verify that the investigational device (LatGYNious) is appropriate to significantly improve the pelvic organ prolapse in patients.",[56,27,57,58],"Pelvic Organ Prolapse (POP)","Uterus Prolapse","Laparoscopic Surgery",[60],"Laparoscopic lateral suspension (LLS)","2025-07-15",{"date":63,"type":35},"2025-07-18",{"date":65,"type":35},"2025-07-01",{"date":67,"type":21},"2027-07",{"name":69,"class":70},"A.M.I. Agency for Medical Innovations GmbH","INDUSTRY",5,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":80,"targetDuration":82,"studyType":83,"phases":4,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":42},"100333021","pessary-satisfaction-criteria-for-urogenital-prolapse-100333021","NCT03615872","Pessary Satisfaction Criteria for Urogenital Prolapse","Evaluation of Patient Satisfaction With Pessary in the Treatment of Genital Prolapse","PeSaCUP","Inclusion Criteria:\n\n* The research protocol will be proposed to all patients with a symptomatic genital prolapse, over 18 years of age, who speak French and who agree to participate in this study\n* Prolapse defined according to the International Classification POP-Q-.\n\nExclusion Criteria:\n\n* Minors under 18 years of age\n* Pregnant or lactating women\n* Women Not speaking French (the good understanding of French is necessary to answer questionnaires and for informed information)\n* Women unable to understand due to cognitive impairment or degenerative disease (dementia\u002F Alzheimer's disease)",{"count":81,"type":21},150,"5 Years","OBSERVATIONAL","Genital prolapse is a common pathology with a prevalence ranging from 2.9 to 11.4% or 31.8% to 97.7%, depending on whether a questionnaire or clinical examination is used. The use of pessary in the treatment of prolapse remains discussed despite a satisfaction rate of 50 to 80% in the literature and a minimal complications rate.\n\nThe main objective of this study is to assess the satisfaction of patients carrying a pessary in the first year after the laying.",[27,86,87],"Pessary","Satisfaction",[89,90],"quality of life","efficiency","2024-09-19",{"date":93,"type":35},"2024-09-20",{"date":95,"type":35},"2018-06-20",{"date":97,"type":21},"2025-06",{"name":99,"class":41},"University Hospital, Caen"]