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TURP Outcome Prediction Calculator Study

NCT07277556 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-12-19

No results posted yet for this study

Summary

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.

Conditions

  • Benign Prostatic Hyperplasia (BPH)

Sponsors & Collaborators

  • General Hospital Sveti Duh

    lead OTHER

Principal Investigators

  • Adelina Hrkac, MD · Klinička bolnica "Sveti Duh", Zavod za urologiju

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-02
Primary Completion
2027-03-01
Completion
2027-12-13

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07277556 on ClinicalTrials.gov