[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"benign-prostatic-hyperplasia-with-symptomatic-lower-urinary-tract-symptoms\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:benign-prostatic-hyperplasia-with-symptomatic-lower-urinary-tract-symptoms":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100639152","anesthesia-type-and-holep-outcomes-a-multi-center-study-100639152",false,"NCT07585552","Anesthesia Type and HoLEP Outcomes: A Multi-Center Study","Does Anesthesia Type Affect HoLEP Outcomes? A Multi-Center, Real-World Comparative Study","Inclusion Criteria:\n\n* 18 years or older men who have BPO requiring surgical treatment.\n* Participants who can give written informed consent.\n* Having no more than 3 points for the American Society of Anesthesiologists (ASA) physical status classification scale (ASA 1 to 3).\n\nExclusion Criteria:\n\n* Absolute contraindication for spinal or general anesthesia\n* History of previous surgery for prostate (e.g., surgery for prostate cancer, surgery for benign prostate obstruction)\n* Uncorrected bleeding disorder (INR \\> 1.5)\n* Participants who are not willing to give informed consent.\n* Participants who have a proven urinary tract infection at the time of the surgery.\n* Participants who are not able to be contacted for regular follow-ups.","MALE","18 Years",{"count":19,"type":20},320,"ESTIMATED","OBSERVATIONAL","1. What is this study about, and why is it required?\n\n   The goal of this observational study is to learn if anesthesia type (e.g., general anesthesia, spinal anesthesia) affects the safety and efficiency of HoLEP surgery. The main question it aims to answer is:\n\n   \\- Is a particular type of anesthesia related to less or more bleeding during the surgery?\n2. What will be assessed to answer the main question of this study? (Outcome measure(s))\n\n   2.1. Primary outcome measure of this study is:\n\n   \\- Change in the hemoglobin level perioperatively.\n\n   2.2. Secondary outcome measures are:\n   * Requirement for the usage of any vasoactive medication due to low blood pressure\n   * Time passed until discharge.\n   * Time passed until the removal of the bladder drainage catheter.\n   * Ratio of the unwanted events that require additional intervention other than medication, fluids, or blood transfusions (Complications, Clavien-Dindo Grade III or higher).\n   * International symptom questionnaire score 3 months after surgery.\n   * Quality of life (QoL) score 3 months after surgery.\n   * Peak urinary current velocity (Qmax) and post-void residual volume measurement 3 months after surgery.\n3. Can anyone participate in this study?\n\nVoluntary participants should meet the following criteria:\n\n* Being older than 18 years old.\n* Having bothersome lower urinary tract symptoms due to prostatic enlargement requiring surgical treatment.\n* Having no untreated or uncontrolled systemic disease, which refers to having an ASA (American Society of Anesthesiologists Physical Status Classification System) score III at most.",[24],"Benign Prostatic Hyperplasia With Symptomatic Lower Urinary Tract Symptoms",[26,27,28,29,30],"HoLEP","Benign Prostate Obstruciton (BPO)","Male LUTS","Real World Study","Observational Study","NOT_YET_RECRUITING","2026-05-09",{"date":34,"type":35},"2026-05-13","ACTUAL",{"date":37,"type":20},"2026-04-23",{"date":39,"type":20},"2027-09-01",{"name":41,"class":42},"Ondokuz Mayıs University","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":64,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":43},"100591670","bipolar-resection-vs-enucleation-of-prostate-100591670","NCT06983444","Bipolar Resection vs Enucleation of Prostate","Bipolar Trans Urethral Resection of the Prostate (TURP) Versus Bipolar Enucleation of the Prostate in Treatment of Benign Prostatic Hyperplasia (BPH): A Prospective Randomized Comparative Clinical Study","TURP vs BiTUEP","Inclusion Criteria:\n\n1. Patients with lower urinary tract symptoms (LUTS) due to BPH.\n2. Patients with international prostate score system (IPSS) more than 8.\n3. Patients with maximal urinary flow rate (Qmax) less than 10ml\u002Fsecond.\n4. Patients with Prostatic volume (60 - 100 gm).\n5. Patient with indication for surgical intervention.\n6. Patient age (50-80 years old)\n\nExclusion Criteria:\n\n1. Prostatic cancer.\n2. Bladder cancer.\n3. Urethral stricture.\n4. Neurogenic bladder.","50 Years","80 Years",{"count":55,"type":20},100,"INTERVENTIONAL",[58],"NA","The aim of this study is to evaluate efficacy and safety of transurethral resection of the prostate and bipolar enucleation of the prostate.",[61,62,24,63],"Benign Prostatic Hyperplasia (BPH) Requiring Surgical Resection","Benign Prostatic Hyperplasia With Outflow Obstruction","Benign Prostatic Hyperplasia With Lower Urinary Tract Symptoms",[65,66,67],"TURP","TUEP","BPH","RECRUITING","2025-05-17",{"date":71,"type":35},"2025-05-21",{"date":73,"type":20},"2025-06-01",{"date":75,"type":20},"2026-07",{"name":77,"class":42},"South Valley University"]