Comparison between laparoscopic (keyhole surgery) and robot-assisted surgery for patients with prostate cancer
Not Applicable
Completed
- Conditions
- Surgical treatment of localized prostate cancerSurgery
- Registration Number
- ISRCTN11552140
- Lead Sponsor
- niversity of Turin
- Brief Summary
2012 Results article in https://pubmed.ncbi.nlm.nih.gov/22840353/ (added 21/04/2022) 2024 Results article in https://doi.org/10.1002/pros.24702 Ten-year follow up (added 04/04/2024)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Male
- Target Recruitment
- 120
Inclusion Criteria
1. Aged between 50 and 75 years
2. Diagnosed with localised or locally advanced prostate adenocarcinoma (clinical stage T1-2 or T3, in each case N0, M0)
3. Gleason score between 2 and 10
4. PSA <20ng/ml
Exclusion Criteria
Patients who withdraw consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Postoperative urinary continence will be assessed with ICS questionnaire at 1, 3, 6, 12, 60 and 120 months after surgery.<br>2. Postoperative erectile function will be assessed with IIEF5 questionnaire at 1, 3, 6, 12, 60 and 120 months after surgery.
- Secondary Outcome Measures
Name Time Method 1. Serum PSA levels will be assessed at 1, 3, 6, 12, 60 and 120 months after surgery<br>2. Intraoperative complications will be assessed using Clavien-Dindo scale during the intervention<br>3. Postoperative complications will be assessed using Clavien-Dindo scale at 1, 12, 60 and 120 months after surgery