Actively Recruiting
Voiding and Erectile Function After Retroperitoneal Lymph Node Dissection for Testicular Cancer
Led by Jagiellonian University · Updated on 2025-07-16
20
Participants Needed
1
Research Sites
133 weeks
Total Duration
On this page
AI-Summary
What this Trial Is 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.
CONDITIONS
Official Title
Voiding and Erectile Function After Retroperitoneal Lymph Node Dissection for Testicular Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult male with testicular cancer undergoing retroperitoneal lymph node dissection (RPLND)
You will not qualify if you...
- History of retroperitoneal lymph node dissection (RPLND) surgery
- Lack of consent
AI-Screening
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Trial Site Locations
Total: 1 location
1
Jagiellonian University Medical College
Krakow, Malopolska, Poland, 30-688
Actively Recruiting
Research Team
A
Anna K. Czech, M.D., Ph.D.
CONTACT
J
Jakub Frydrych, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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