[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"urgency-incontinence\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:urgency-incontinence":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100622559","defining-ileorectal-syndrome-a-prospective-observational-study-100622559",false,"NCT07385196","Defining Ileorectal Syndrome: a Prospective Observational Study","Trying to Define Ileorectal Syndrome: a Prospective Observational Study","DEFINE-IRS","Inclusion Criteria: Age ≥18 years\n\nHistory of ileorectal anastomosis or preserved rectum following colorectal surgery\n\nAbility to understand the study procedures and provide written informed consent\n\nWillingness to participate in prospective follow-up assessments -\n\nExclusion Criteria:\n\nAge \\\u003C18 years\n\nPermanent stoma\n\nTotal rectal excision\n\nInability to complete follow-up assessments\n\n\\-","ALL","18 Years",{"count":20,"type":21},30,"ESTIMATED","10 Days","OBSERVATIONAL","1. Study Title: Trying to Define Ilorectal Syndrome: A Prospective Observational Study\n2. Study Objective and Significance:\n\n   Primary Objective:\n\n   To prospectively evaluate the frequency, symptom severity, and impact on quality of life of ileorectal syndrome developing in patients who have undergone total colectomy and ileorectal anastomosis.\n\n   Secondary Objectives:\n   * To examine the relationship between postoperative bowel dysfunction and quality of life\n   * To investigate clinical factors affecting symptom severity This study aims to contribute to postoperative follow-up and management strategies by revealing patient-centered outcomes of ileorectal syndrome.\n3. Expected Benefits and Risks of the Study:\n\n   Expected Benefits\n   * Prospective and systematic evaluation of ileorectal syndrome\n   * Identification of factors affecting the quality of life of these patients\n   * Increased awareness in clinical follow-up Potential Risks\n   * The study is observational and questionnaire-based and does not involve additional medical risks\n   * No invasive procedures will be performed on the patients\n4. Type, scope, and design of the planned study:\n\n   * Type: Prospective, observational\n   * Scope: Single-center\n   * Design: Questionnaire-based clinical trial\n5. Number of patients and volunteers to be included in the study, their qualifications, and the rationale for selection:\n\n   * Total number of patients: 30\n   * Age range: ≥18 years\n   * Gender: Female and male This number was determined based on the appropriate patient population followed in our center.\n6. Parameters to be examined:\n\n   Demographic data (age, gender, BMI) Surgical indication Whether the surgery was performed openly or laparoscopically Level of anastomosis Maximum daily bowel movement frequency and duration Feeling of urgency Nocturnal bowel movements Fluid\u002Fgas incontinence - soiling Ileus in ADBG Whether electrolyte abnormalities developed Length of hospital stay Need for re-hospitalization Severity of symptoms based on patient reports and questionnaire questions\n7. Where and by whom the parameters will be examined\n\n   Data will be collected by the responsible investigator at the relevant clinic.\n8. Which parameters to be used in the study are routine for that disease group and which are specific to the study?\n\n   Routine: Demographic data, surgical information, laboratory results Study-Specific: Postoperative bowel functionality, symptom questionnaire\n9. Estimated study duration, start and end dates:\n\n   Start date: 1\u002F1\u002F2026 End date: 31\u002F12\u002F2026 Total duration: 12 months\n10. Inclusion, exclusion, and withdrawal criteria:\n\n    Inclusion Criteria\n    * Having undergone total colectomy and ileorectal anastomosis\n    * 18 years of age and older\n    * Providing written informed consent Exclusion Criteria\n    * Serious neurological disease affecting bowel function\n    * Patients with incomplete follow-up data Withdrawal\n    * At the patient's request\n    * If follow-up cannot be completed\n11. Termination criteria:\n\n    By the ethics committee Termination decision Unforeseen circumstances preventing the conduct of the study\n12. Statistical methods to be used in the evaluation of the data to be obtained as a result of the research:\n\n    * Descriptive statistics (mean, median, percentage)\n    * Parametric and non-parametric tests\n    * Analysis of the relationship between symptom severity and quality of life\n    * p \\\u003C 0.05 statistical significance level",[26,27,28,29],"Total Colectomy","Diarrhea","Urgency Incontinence","Soilings, Fecal","RECRUITING","2026-01-27",{"date":33,"type":34},"2026-02-03","ACTUAL",{"date":36,"type":34},"2025-12-19",{"date":38,"type":21},"2027-02-15",{"name":40,"class":41},"Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":49,"minAge":18,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":42},"100595927","implementation-of-the-app-ttii-for-treatment-of-urgency-and-mixed-urinary-incontinence-100595927","NCT07038811","Implementation of the App Tät®II for Treatment of Urgency and Mixed Urinary Incontinence","Inclusion Criteria:\n\n* Female gender\n* Age ≥18 years\n* Symptoms of urgency urinary incontinence or mixed urinary incontinence\n* Medical evaluation and documentation of urinary incontinence by ordinary doctor\n* Signed informed consent\n\nExclusion Criteria:\n\n* Pregnancy\n* Childbirth in the last 6 months\n* Painful urges\n* Difficulties emptying the bladder\n* Blood in urine\n* Need of further investigation concerning the urinary incontinence, according to the clinical doctor","FEMALE",{"count":51,"type":21},60,"This observational study aims to evaluate the implementation and use of the Tät®II app for the treatment of urgency and mixed urinary incontinence in women over the age of 18 after contact with ordinary healthcare, as well as its effectiveness. The study aims to answer the following question:\n\nIs treatment via the app effective and feasible after primary care?\n\nParticipants will use the app for 15 weeks to treat urgency and mixed urinary incontinence. They will answer online survey questions about their urinary incontinence before, after 15 weeks, and one year after treatment.",[28,54],"Mixed Incontinence, Urge and Stress",[56,57],"urinary incontinence","app treatment","2025-06-23",{"date":60,"type":34},"2025-06-26",{"date":62,"type":34},"2025-06-12",{"date":64,"type":21},"2027-06-01",{"name":66,"class":41},"Umeå University"]