TURP Outcome Prediction Calculator Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorGeneral Hospital Sveti Duh

About this trial

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:

Which preoperative parameters (IPSS, prostate volume, post-void residual urine, Qmax, comorbidities) are associated with successful postoperative outcomes?

Can these parameters be used to develop a non-invasive calculator to estimate the likelihood of TURP success?

Participants will undergo routine clinical evaluation that is part of standard care, including:

* completion of the IPSS questionnaire * digital rectal examination * ultrasound measurement of prostate volume and residual urine * uroflowmetry (Qmax and voided volume) * standard laboratory testing Eligible participants will then undergo TURP as clinically indicated and return for postoperative assessments of symptom improvement and urinary flow parameters.

Eligibility criteria

Qualifiers

Male patients aged 18 years or older

Clinical diagnosis of benign prostatic hyperplasia (BPH)

Indication for TURP based on symptoms or complications

Completed preoperative evaluation (IPSS, ultrasound, PSA, uroflowmetry)

Disqualifiers

Suspected or confirmed prostate cancer

No clinical evidence of BPH

Prior urodynamic diagnosis of underactive/neurogenic bladder

Prior prostate surgery

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations

Sponsors and collaborators