[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"prolapse\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:prolapse":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100568315","a-telehealth-intervention-to-increase-patient-preparedness-for-surgery-in-latinas-100568315",false,"NCT06679621","A Telehealth Intervention to Increase Patient Preparedness for Surgery in Latinas","TIPPS-Urogyn","Inclusion Criteria:\n\nPatients who\n\n* Self-report as female\n* 18 years and older\n* Self-report as Hispanic ethnicity\n* Scheduled to undergo a surgery for a urogynecologic condition in the operating room (surgery to correct pelvic organ prolapse, urinary\u002Ffecal incontinence, fistula, urethral masses)\n* Able to read and write English and\u002For Spanish\n\nUrogynecologists who -Routinely perform urogynecologist surgeries to correct pelvic organ prolapse, urinary\u002Ffecal incontinence, fistula, urethral masses\n\nNurses who\n\n* Spend most of their time at a urogynecologic clinic\n* Engage in the process of preparing patients for urogynecologic surgery\n\nExclusion Criteria:\n\nPatients who\n\n* Self-report as male\n* Are less than 18 years of age\n* Self-report as not of Hispanic ethnicity\n* Scheduled to undergo a surgery for a condition that is not urogynecologic or is not in the operating room\n* Patients undergoing procedures that are traditionally performed in the office (bladder Botox, pelvic floor Botox, urethral bulking)\n\nUrogynecologists who\n\n-Do not routinely perform urogynecologic surgery\n\nNurses who\n\n* Do not spend most of their time at a urogynecology clinic\n* Do not engage in the process of preparing patients for urogynecologic surgery",true,"FEMALE","18 Years",{"count":20,"type":21},357,"ESTIMATED","INTERVENTIONAL",[24],"NA","There are 3 aims of this study. In Aim 1 community patient partners will be enrolled to help guide the research being performed in all of the aims. Investigators will also administer a survey that will help determine factors associated with surgical preparedness. In Aim 2 investigators will develop an intervention to increase surgical preparedness using Human Centered Design Methods. Aim 3 will pilot test the intervention using mixed methods to determine feasibility and implementation outcomes.",[27,28],"Incontinence","Prolapse","RECRUITING","2026-08-12",{"date":32,"type":33},"2026-08-14","ACTUAL",{"date":35,"type":33},"2024-11-01",{"date":37,"type":21},"2027-06-01",{"name":39,"class":40},"University of Alabama at Birmingham","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":66,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":41},"100549201","biological-ovitex-versus-synthetic-graft-in-robotic-prolapse-surgery-100549201","NCT06430931","Biological OviTex Versus Synthetic Graft in Robotic Prolapse Surgery","Biological OviTex Versus Synthetic Graft in Robotic Prolapse Surgery: a Multicentre, Phase 11-111, Partially Randomised Patient Preference Trial","ProTex","Inclusion Criteria:\n\n* Indication for VMR or SCR set by the treating surgeon\u002Fgynecologist in accordance to the current guidelines on rectal and pelvic prolapse;\n* Counselled for therapeutic options and given informed consent for VMR or SCR;\n* Counselled for different types of mesh (OviTex or Prolene) and randomisation;\n* Written informed consent for randomisation, OviTex implant or Prolene;\n* Written informed consent for observational data collection.\n\nExclusion Criteria:\n\n* Mentally incompetent patients (unable to fulfil questionnaires).\n* Allergy to ovine rumen.\n* A medical history of pelvic radiation therapy.\n* Scheduled for a redo-rectopexy.\n* A medical history of previously implanted pelvic floor meshes or native tissue.\n* Language barrier","ALL",{"count":52,"type":21},184,[24],"This prospective study aims to assess the efficacy of the OviTex 1S permanent mesh in pelvic floor surgery in comparison with the current standard polypropylene mesh.",[56,28,57,58,59,60,61,62,63,64,65],"Colorectal Disorders","Prolapse Rectal","Prolapse Genital","Prolapse Pelvic","Rectocele","Prolapse Uterus","Cystocele","Enterocele","Prolapse Bladder","Prolapse; Cervix",[28,67,68,69,70,71],"Abdominal prolapse Surgery","Biological mesh","OviTex","VMR","sacrocolporectopexy","2025-12-31",{"date":74,"type":33},"2026-01-02",{"date":76,"type":33},"2023-12-06",{"date":78,"type":21},"2027-07-01",{"name":80,"class":40},"Meander Medical Center"]