Trials / Completed
CompletedNCT04037800
An RCT to Compare Early Continence Recovery After RARP With or Without Sustainable Functional Urethral Reconstruction
Impact of Sustainable Functional Urethral Reconstruction on Early Continence Recovery After Robotic-assisted Radical Prostatectomy: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 96 (actual)
- Sponsor
- Changhai Hospital · Academic / Other
- Sex
- Male
- Age
- 40 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The study is a prospective randomized controlled trail to compare early urinary continence recovery after robotic-assisted radical prostatectomy with or without sustainable functional urethral reconstruction (SFUR).
Detailed description
Early urinary incontinence has always been a tricky problem for both patients and urologists, even though over 90% patients can recover 1 year after surgery. Many urologists are trying to modify the surgical technique to resolve this problem. Sustainable functional urethral reconstruction (SFUR) is a novel technique which may improve early urinary continence recovery for both local and locally advanced prostate cancer, and even for those with high volume prostate by providing adequate urethral length with bladder neck tubularization and making sustainable periurethral support with peritoneal flap. The purpose of this study is to verify the impact of this new technique on early recovery of urinary continence, as well as on urinary function and oncological outcomes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | SFUR-RARP | Robotic-assisted radical prostatectomy with sustainable functional urethral reconstruction (SFUR) |
| PROCEDURE | Standard RARP | Robotic-assisted radical prostatectomy with conventional RARP procedures. |
Timeline
- Start date
- 2019-12-08
- Primary completion
- 2021-01-10
- Completion
- 2021-09-28
- First posted
- 2019-07-30
- Last updated
- 2022-05-18
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04037800. Inclusion in this directory is not an endorsement.