[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100614281":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":7,"responsibleParty":18,"collaborators":7,"id":21,"slug":22,"hasResults":23,"nctId":24,"briefTitle":25,"officialTitle":26,"acronym":27,"eligibilityCriteria":28,"healthyVolunteers":23,"sex":29,"minAge":30,"maxAge":7,"enrollmentInfo":31,"targetDuration":7,"studyType":34,"phases":7,"briefSummary":35,"conditions":36,"keywords":38,"overallStatus":45,"whyStopped":7,"lastUpdateSubmitDate":46,"lastUpdatePostDateStruct":47,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":7},{"fullName":5,"class":6},"General Hospital Sveti Duh","OTHER",null,[9],{"name":10,"affiliation":11,"role":12},"Adelina Hrkac, MD","Klinička bolnica \"Sveti Duh\", Zavod za urologiju","PRINCIPAL_INVESTIGATOR",[14],{"name":10,"role":15,"phone":16,"phoneExt":7,"email":17},"CONTACT","00385958146992","adelina.surjan@gmail.com",{"type":12,"investigatorFullName":19,"investigatorTitle":20,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"Adelina Hrkac","MD, FEBU, Principal Investigator","100614281","turp-outcome-prediction-calculator-study-100614281",false,"NCT07277556","TURP Outcome Prediction Calculator Study","Identification of Predictive Parameters for Developing a TURP Outcome Calculator for Preoperative Patient Assessment","TURP-SCORE","Inclusion Criteria:\n\n* Male patients aged 18 years or older\n* Clinical diagnosis of benign prostatic hyperplasia (BPH)\n* Indication for TURP based on symptoms or complications\n* Completed preoperative evaluation (IPSS, ultrasound, PSA, uroflowmetry)\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Suspected or confirmed prostate cancer\n* No clinical evidence of BPH\n* Prior urodynamic diagnosis of underactive\u002Fneurogenic bladder\n* Prior prostate surgery\n* Inability to participate in follow-up","MALE","18 Years",{"count":32,"type":33},200,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to identify which preoperative clinical, ultrasound, and uroflowmetry parameters can help predict the success of transurethral resection of the prostate (TURP) in adult male patients with symptomatic benign prostatic hyperplasia (BPH). The main questions it aims to answer are:\n\nWhich preoperative parameters (IPSS, prostate volume, post-void residual urine, Qmax, comorbidities) are associated with successful postoperative outcomes?\n\nCan these parameters be used to develop a non-invasive calculator to estimate the likelihood of TURP success?\n\nParticipants will undergo routine clinical evaluation that is part of standard care, including:\n\n* completion of the IPSS questionnaire\n* digital rectal examination\n* ultrasound measurement of prostate volume and residual urine\n* uroflowmetry (Qmax and voided volume)\n* standard laboratory testing Eligible participants will then undergo TURP as clinically indicated and return for postoperative assessments of symptom improvement and urinary flow parameters.",[37],"Benign Prostatic Hyperplasia (BPH)",[39,40,41,42,43,44],"BPH","LUTS","TURP","Uroflowmetry","IPSS","Outcome Prediction","NOT_YET_RECRUITING","2025-12-15",{"date":48,"type":49},"2025-12-19","ACTUAL",{"date":51,"type":33},"2026-03-02",{"date":53,"type":33},"2027-12-13",{"name":5,"class":6}]