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Clinical Trials in Poland / NCT06985004
Active, not recruiting Observational

Predicting Operational Difficulties and Outcomes of RARP Based on Preoperative Assessment - Introducing the PIODO Questionnaire

NCT06985004 · tracked via the Priya Life Science Poland tracker
Phase
Observational
Started
2024-01-01
Last updated
2025-05-22

Condition(s) studied

Prostate CancerRobot-Assisted Laparoscopic Radical Prostatectomy

Investigational drug(s) / intervention(s)

PIODO Questionnaire

PIODO Questionnaire: An original PIODO Questionnaire is a structured protocol that has been developed by the investigators of this study for the preoperative assessment of patients undergoing RARP. It evaluates not only clinical data on the prostate cancer, but also patient characteristics, including anthropometric measurements of the pelvis. The aim is to develope a tool that can be used to predict the risk of operational difficulties and possible outcomes of RARP.

Study summary

The goal of this observational study is to learn about the factors that affect the course of robot-assisted radical prostatectomy and have an impact on functional and oncological outcomes in patients undergoing RARP. The main question it aims to answer is:

• Can the investigators predict the occurrence of operational difficulties and outcomes of RARP based on preoperative assessment including body habitus and pelvimetry?

Participants undergoing RARP will be assessed preoperatively with the use of a PIODO Questionnaire, a structured protocol of preoperative assessment focusing on clinical data and MRI pelvic measurements to evaluate if the investigators can predict the risk of operational difficulties and possible outcomes of RARP. In a 1 year follow-up the investigators will collect data on functional and oncological outcomes.

Eligibility

Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with prostate cancer undergoing RARP. Exclusion Criteria: * Neoadjuvant androgen deprivation therapy before RARP. * Lack of consent for study participation or willingness to comply with all procedures and assessments.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Urology and Urological Oncology Szczecin Poland

More Pomeranian Medical University Szczecin trials in Poland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06985004 on ClinicalTrials.gov ↗ ← All trials in Poland