prostate carcinoma
Conditions
Interventions
Control Group:Current standard surgical treatment for localized prostate cancer,tandard radical prostatectomy without any form of suspension or additional support r
Treatment Group:Standard radical prostatectomy + real-time urethral pressure monitoring-guided autologous vas deferens bladder neck urethral suspension
Sponsors
The First Affiliated Hospital of Soochow University
Eligibility
Sex/Gender
Male
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Age <= 80 years; 2. Pathologically confirmed prostate cancer and scheduled to undergo radical prostatectomy; 3. Clinical stage T1c-T2cN0M0; 4. American Society of Anesthesiologists (ASA) classification Grade I-III; 5. Voluntary participation in this study and provision of written informed consent.
Exclusion criteria
Exclusion criteria: 1.History of pelvic radiotherapy or prostate surgery; 2.Preoperative urinary incontinence or routine use of pads; 3.Severe neurogenic bladder dysfunction; 4.Untreated urethral stricture or bladder neck contracture; 5.Severe mental illness that may interfere with follow-up compliance; 6.History of allergy to sutures or absorbable materials used in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pad-free rate at 1 month postoperatively; | — |
Secondary
| Measure | Time frame |
|---|---|
| IPSS score;ICI-Q-SF score;Number of pads used; | — |
Countries
China
Contacts
Public ContactHuang Yuhua
The First Affiliated Hospital of Soochow University
Outcome results
None listed