[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Dr. Lutfi Kirdar Kartal Training and Research Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":133},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,50,77,108],{"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":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100617736","comparison-of-video-based-phone-app-vs-supervised-preoperative-exercise-for-acl-reconstruction-100617736",false,"NCT07322497","Comparison of Video Based Phone App vs. Supervised Preoperative Exercise for ACL Reconstruction","Investigation of the Effects of Video Based Physical Exercise and Physiotherapist Supervised Physical Exercise Before Anterior Cruciate Ligament Reconstruction","ACL-PREHAB-APP","Inclusion Criteria:\n\n* Patients with a diagnosed unilateral Anterior Cruciate Ligament (ACL) rupture\n* Patients scheduled for ACL reconstruction surgery.\n* Age between 18 and 45 years.\n* Patients willing to participate and sign the informed consent form.\n\nExclusion Criteria:\n\n* Patients with multiple ligament injuries (e.g., combined ACL and PCL\u002FMCL injury).\n* Patients with bilateral ACL injuries.\n* Presence of accompanying fractures around the knee joint.\n* Presence of active infection.\n* Patients who refuse surgery or withdraw consent.","ALL","18 Years","45 Years",{"count":21,"type":22},66,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn if using a phone app for exercises is as effective as working with a physical therapist before anterior cruciate ligament knee surgery. It will also check if exercising before surgery helps patients recover better compared to those who do not follow a specific exercise plan. The main questions it aims to answer are:\n\n* Does the phone app help patients improve their knee strength and movement as well as seeing a physical therapist?\n* Do patients who exercise before surgery have a better recovery after surgery than those who do not?\n\nResearchers will compare the phone app group to a physical therapist group and a group with no specific exercise plan to see which method works best.\n\nParticipants will:\n\n* Follow an exercise plan for 4 weeks before their surgery (either using the app, with a therapist, or no specific plan).\n* Visit the clinic for check-ups before starting the exercises, right before the surgery, and 6 months after the surgery.\n* Complete simple tests and surveys to measure their knee health.",[28,29,30],"Anterior Cruciate Ligament (ACL) Rupture","Anterior Cruciate Ligament (ACL) Reconstruction","Anterior Cruciate Ligament (ACL) Injury",[32,33,34,35,36],"Preoperative Rehabilitation","ACL Reconstruciton","Prehabilitation","Mobile Application","Telerehabiltiation","NOT_YET_RECRUITING","2025-12-22",{"date":40,"type":41},"2026-01-07","ACTUAL",{"date":43,"type":22},"2025-12-29",{"date":45,"type":22},"2027-12-29",{"name":47,"class":48},"Dr. Lutfi Kirdar Kartal Training and Research Hospital","OTHER_GOV",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":49},"100590522","phase-4-comparison-of-the-effectiveness-of-oral-and-intratympanic-corticosteroid-treatments-in-patients-diagnosed-with-sudden-sensorineural-hearing-loss-100590522","NCT06968507","Comparison of the Effectiveness of Oral and Intratympanic Corticosteroid Treatments in Patients Diagnosed With Sudden Sensorineural Hearing Loss","Inclusion Criteria:\n\n* 18 years of age and older\n* Unilateral sudden sensorineural hearing loss that developed within 72 hours and has lasted for 14 days or less\n* Affected side PTA (500-100-2000-4000hz) should be over 50dB\n* Affected side should be at least 30dB lower than healthy side in 3 frequencies\n* Hearing should be symmetrical according to patient's statement before sensorineural hearing loss\n* If used, steroid use should be less than 10 days\n* Cerebellar and vestibular examination should be normal\n\nExclusion Criteria:\n\n* Having a history of hearing-related surgery other than a ventilation tube\n* Having a history of previous hearing loss, fluctuating hearing or Meniere's disease, chronic inflammatory or suppurative ear disease or cholesteatoma, otosclerosis\n* Being under 18 or over 80\n* Having a history of physical-barotrauma\n* Presence of structural or retrocochlear pathology in the examination and imaging that would explain the unilateral hearing loss\n* Patients diagnosed with tuberculosis or receiving prophylactic tuberculosis treatment, diabetes mellitus, rheumatological patients, those with atherosclerotic disease, serious psychiatric patients, those receiving chemotherapy, radiotherapy or immunosuppressant treatment, pancreatitis patients, HIV, hepatitis C and B patients, those with chronic renal failure, substance abusers, those with active herpetic lesions, severe osteoporosis patients, those with hearing loss within 4 weeks after general anesthesia, those with a history of head and neck cancer.","80 Years",{"count":58,"type":22},214,[60],"PHASE4","The goal of this clinical trial is to learn which one works to treat better in patients with sudden sensorineural hearing loss, oral or intratympanic corticosteroid treatment.\n\nThe main question it aims to answer is:\n\nWhich corticosteroid treatment is more effective in patients with sudden sensorineural hearing loss, oral or intratympanic?\n\n* In our study, it was planned to divide the treatment schemes compared into two groups. Group 1 included patients who received oral methylprednisolone treatment daily for 2 weeks (48 mg for the first 7 days, 32 mg for the following 2 days, 16 mg for the 2 days, and 8 mg for the last 3 days). Group 2 included patients who received intratympanic 8 mg\u002F2 ml dexamethasone every other day, totally 4 doses.\n* Visit the clinic after diagnose in first week, second week, first month and second month for checkups and tests ( temporal MR, odimetric results)",[63],"Sudden Sensorineural Hearing Loss",[65,66,67],"intratympanic dexamethasone","Sudden sensorineural hearing loss","oral methylprednisolone","RECRUITING","2025-05-05",{"date":71,"type":41},"2025-05-13",{"date":73,"type":22},"2025-05-20",{"date":75,"type":22},"2028-09-10",{"name":47,"class":48},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":84,"minAge":85,"maxAge":56,"enrollmentInfo":86,"targetDuration":4,"studyType":23,"phases":88,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":49},"100575779","vnotes-and-vaginal-hysterectomy-for-benign-indications-100575779","NCT06776718","VNOTES and Vaginal Hysterectomy for Benign Indications","Comparison of VNOTES and Vaginal Hysterectomy for Benign Indications","Inclusion Criteria:\n\n* aged between 40 and 80 years\n* undergo hysterectomy for benign gynecological conditions\n\nExclusion Criteria:\n\n* history of urogynecological surgery (including pelvic organ prolapse surgery and mid-urethral sling procedures),\n* suspected gynecologic malignancies,\n* endometriosis,\n* tubal-ovarian abscesses,\n* pelvic organ prolapse exceeding grade 2,\n* individuals who refused to participate in the study","FEMALE","40 Years",{"count":87,"type":22},100,[25],"This study aimed to compare the surgical outcomes of Vaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES) and conventional vaginal hysterectomy (VH) for benign gynecological conditions.\n\nA prospective analysis will conducted at a tertiary hospital from January 2025 to February 2025. Patients aged 40-80 who underwent hysterectomy for benign indications will included. Outcomes will assessed included surgical outcomes, Visual Analog Scale (VAS) pain scores, and complication rates.",[91,92,93],"Hysterectomy","Hysterectomy, Benign Uterine Diseases","Hysterectomy, Vaginal",[95,96,97,98,99],"vNOTES","vaginal hysterectomy","benign gynecology","surgical outcomes","Pain","2025-01-13",{"date":102,"type":41},"2025-01-15",{"date":104,"type":22},"2025-01",{"date":106,"type":22},"2025-02",{"name":47,"class":48},{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":115,"sex":17,"minAge":18,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":49},"100560144","effect-of-exercise-on-clinical-symptoms-cognitive-performance-and-quality-of-life-in-schizophrenia-patients-treated-with-clozapine-100560144","NCT06573320","Effect of Exercise on Clinical Symptoms, Cognitive Performance, and Quality of Life in Schizophrenia Patients Treated With Clozapine","Investigating the Effect of Exercise on Clinical Symptoms, Cognitive Performance, and Quality of Life in Schizophrenia Patients Treated With Clozapine","Inclusion Criteria:\n\n* Patients treated who were diagnosed with schizophrenia according to DSM-V criteria by psychiatrist at the Turkish Ministry of Health Kartal Dr. Lütfi Kırdar City Hospital\n* using a therapeutic dose of 300-500 mg\u002Fday of clozapine,\n\nExclusion Criteria:\n\n* pregnancy",true,"65 Years",{"count":118,"type":22},60,[25],"This prospective study aims to investigate the effects of exercise on clinical symptoms, cognitive performance, and quality of life in schizophrenia patients treated with Clozapine.",[122,123,124],"Schizophrenia","Clozapine","Exercise","2024-08-24",{"date":127,"type":41},"2024-08-27",{"date":129,"type":41},"2024-03-14",{"date":131,"type":22},"2024-08-31",{"name":47,"class":48},""]