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Analysis of Immediate Urinary Continence Predictors After RS-RARP

Analysis of Immediate Urinary Continence Predictors After Retzius-sparing Robot-assisted Radical Prostatectomy: A Single-center Retrospective Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06850116
Enrollment
400
Registered
2025-02-27
Start date
2025-01-01
Completion date
2027-01-01
Last updated
2025-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer (Post Prostatectomy), Retzius-sparing Robot-assisted Radical Prostatectomy, Urinary Continence

Keywords

Retzius-sparing robot-assisted radical prostatectomy, Prostate Cancer, urinary continence

Brief summary

This study is a retrospective, single-center clinical trial. It aims to retrospectively analyze the immediate postoperative urinary continence recovery in prostate cancer patients who underwent Retzius-sparing robot-assisted radical prostatectomy in the investigators' center. Based on the general conditions of patients, relevant perioperative clinical indicators, and parameters related to the sphincter and prostate gland measured by MRI, it explores the influencing factors of immediate urinary continence recovery after Retzius-sparing robot-assisted radical prostatectomy in prostate cancer patients and constructs a relevant prediction model, thereby providing clinical guidance value for predicting immediate postoperative urinary continence recovery.

Interventions

PROCEDURERetzius-sparing robot-assisted radical prostatectomy

Retzius-sparing robot-assisted radical prostatectomy

Sponsors

First Affiliated Hospital of Fujian Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Prostate cancer diagnosed by prostate biopsy and underwent Retzius-sparing robot-assisted radical prostatectomy in the investigators' hospital. * Received plain and contrast-enhanced pelvic or prostate MRI examinations before surgery. * Eastern Cooperative Oncology Group (ECOG) performance status score between 0 and 1. * Complete clinicopathological data. * In good general condition, without infections, autoimmune diseases, hematological diseases or other malignant tumors. * Complete postoperative follow-up data, with a postoperative follow-up time of no less than 6 months.

Exclusion criteria

* The patient has surgical contraindications. * The patient has contraindications for MRI examination. * Preoperative presence of congenital urinary system malformations, urinary incontinence or severe lower urinary tract symptoms, and with a history of urinary catheter or previous transurethral resection of the prostate (TURP) surgery. * Having received neoadjuvant treatments that may affect the results of this study, such as radiotherapy or hormonal therapy. * The patient has other concurrent malignant tumors. * The patient has delayed extubation (\> 14 days). * The patient's clinical, imaging and pathological data are incomplete or the patient is lost to follow-up.

Design outcomes

Primary

MeasureTime frameDescription
rate of continencerate of the preservation of urinary control function at 1 week after postoperative removal of the urinary catheter statusTime Frame: 1 week after postoperative removal of the urinary catheter

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026