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Voiding and Erectile Function After Retroperitoneal Lymph Node Dissection for Testicular Cancer (VEEF-RPLND-TC)

J

Jagiellonian University

Status

Enrolling

Conditions

Testicular Cancer

Treatments

Diagnostic Test: Uroflowmetry and questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT06954233
VEEF-RPLND-TC

Details and patient eligibility

About

This study aims to evaluate how retroperitoneal lymph node dissection (RPLND), a surgical treatment for testicular cancer, may affect urinary and sexual functions in men. RPLND involves the removal of lymph nodes from the abdominal area and is sometimes necessary in patients who are not eligible for chemotherapy or who have residual disease after chemotherapy. While this surgery is known to carry a risk of affecting ejaculation, its potential impact on other areas such as urination or erection is not well understood.

The study will prospectively follow adult men undergoing RPLND. It will assess changes in lower urinary tract symptoms, urine flow, ejaculation, erection, and overall quality of life before surgery and during follow-up visits up to 6 months after the operation. Patients will complete standardized questionnaires and undergo simple, non-invasive tests such as urine flow measurement.

By identifying how RPLND may influence urinary and sexual health, this study seeks to improve understanding of the full range of effects of this treatment. The findings may help clinicians better inform patients before surgery and support improved post-operative care.

Full description

This is a prospective observational study designed to evaluate the impact of retroperitoneal lymph node dissection (RPLND) on lower urinary tract and sexual function in patients treated for testicular cancer. The study incorporates validated patient-reported outcome measures (PROMs) alongside objective functional assessments to characterize post-RPLND urinary and sexual sequelae over time.

Patients will complete standardized questionnaires preoperatively and at scheduled postoperative intervals, including the International Prostate Symptom Score (IPSS), International Consultation on Incontinence Questionnaire - Male Lower Urinary Tract Symptoms (ICIQ-MLUTS), International Index of Erectile Function (IIEF-5), Male Sexual Health Questionnaire - Ejaculatory Dysfunction (MSHQ-EjD), and EQ-5D-5L for health-related quality of life. Objective evaluation will include uroflowmetry and ultrasound-based measurement of post-void residual volume.

Enrollment

20 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult male with testicular cancer undergoing retroperitoneal lymph node dissection (RPLND)

Exclusion criteria

  • History of RPLND
  • Lack of consent

Trial design

20 participants in 1 patient group

Adult men with testicular cancer undergoing retroperitoneal lymph node dissection
Description:
Adult men with testicular cancer undergoing retroperitoneal lymph node dissection will have uroflowmetry performed and will complete questionnaires focusing on urinary, erectile and ejaculatory function before surgery, after surgery and during 6 months follow-up
Treatment:
Diagnostic Test: Uroflowmetry and questionnaires

Trial contacts and locations

1

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Central trial contact

Anna K. Czech, M.D., Ph.D.; Jakub Frydrych, M.D.

Data sourced from clinicaltrials.gov

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