Are We Improving Erectile Function Recovery After Radical Prostatectomy? Analysis of Patients Treated over the Last Decade.
Paolo Capogrosso, Emily A Vertosick, Nicole E Benfante...
https://pubmed.ncbi.nlm.nih.gov/30237021/Actively Recruiting
Led by Henry Ford Health System · Updated on 2026-01-16
160
Participants Needed
1
Research Sites
52 weeks
Total Duration
This trial investigates treatments for men with low- and intermediate-risk prostate cancer, comparing two surgical approaches radical prostatectomy RP and precision prostatectomy PP. RP is the current standard surgery that removes the entire prostate and surrounding tissue but often leads to side effects like erectile dysfunction and urinary incontinence. PP is a newer technique that removes most prostate tissue while preserving nerves and structures important for sexual function and continence, aiming to improve quality of life without sacrificing cancer control. Participants will be randomly assigned to receive either standard RP or PP surgery. RP involves complete removal of the prostate and nearby tissue, while PP preserves some prostate tissue and nerves on the side opposite the main cancer lesion. Both surgeries follow similar procedures, require no extra equipment, and are covered by standard health insurance. Outcomes will be measured 12 months after surgery, focusing on sexual health and urinary continence. During the study, participants sexual function will be assessed using the Sexual Health Inventory for Men SHIM score before surgery and at 3 and 12 months after surgery. Urinary continence will also be measured at 12 months by the number of pads used per day. Oncological outcomes will be evaluated by whether additional prostate cancer treatment is needed within 12 months. The study aims to show that PP offers better functional recovery without worse cancer control compared to RP.
CONDITIONS
A Comparison of Radical Prostatectomy and Precision Prostatectomy in Low- and Intermediate-risk Prostate Cancers.
F
Firas Abdollah, MD, FEBU
A
Alex Stephens, MS, MA
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Henry Ford Health System
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | Precision Prostatectomy | Radical Prostatectomy (Standard) |
|---|---|---|
| What it is | Precision Prostatectomy is a surgical technique that aims to remove most cancerous tissue while preserving some prostate tissue and important nerves to help maintain continence and erectile function. | Radical Prostatectomy is the traditional surgery where the entire prostate gland and much surrounding tissue are removed, which may affect urinary continence and erectile function. |
| Role in the trial | Investigational treatment arm assessing outcomes of a nerve- and tissue-sparing surgical technique. | Active comparator arm using standard radical prostatectomy, representing established care. |
| Primary use or reason for selection | Developed to potentially reduce the risks of urinary incontinence and erectile dysfunction by preserving tissue and nerves while still treating localized prostate cancer. | Standard surgery designed to cure localized prostate cancer by removing all cancerous tissue through removal of the prostate and some surrounding structures. |
| How it is performed | Surgical removal of most of the prostate, leaving select tissue and nerves intact on one side to assist with postoperative urinary and sexual function. | Complete removal of the prostate gland and nearby tissues, usually performed as open or minimally invasive surgery. |
| Evidence status | Early published series show feasibility for selected patients and short-term preservation of function in single-center cohorts, but long-term oncological outcomes require confirmation in larger studies. | Extensive evidence supports strong long-term cancer control outcomes; functional recovery (continence and erectile function) varies significantly among patients. |
| Important limitations | Long-term cancer control data are not yet established, and functional outcomes may depend on careful patient selection. Most existing evidence is from single-center, early-phase studies. | May lead to urinary incontinence, erectile dysfunction, or other post-surgical complications. Functional outcomes after surgery can be variable, even with nerve-sparing approaches. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 week
Participants undergo either a Radical Prostatectomy or a Precision Prostatectomy surgical procedure.
1 surgery visit and approximately 1 week of immediate post-operative care visits
Duration - 12 months
Participants are monitored for recovery and outcomes including sexual health and social continence.
Visits at 3 months and 12 months post-surgery
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/24625768/Henry Ford Health System
Lead Sponsor