Evaluating outcomes of robotic surgery for bladder cancer
Impact of Robotic Surgery on Post-operative Outcomes of Patients Who Underwent Radical Cystectomy
This study is testing how well robotic surgery for bladder cancer works compared to traditional surgery by looking at patients' recovery and outcomes over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Florence Academic / other |
| Locations | 1 site (Florence, Tuscany) |
| Trial ID | NCT04900558 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the long-term outcomes of patients undergoing radical cystectomy for bladder cancer, comparing results between robotic and open surgical approaches. It involves collecting data on perioperative, oncological, and functional results to understand the impact of robotic surgery in this context. Patients who are eligible and consent to participate will be monitored throughout their treatment process to gather comprehensive data on their recovery and outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are scheduled to undergo radical cystectomy for bladder cancer.
Not a fit: Patients who are unwilling to participate or refuse consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness and advantages of robotic surgery for bladder cancer patients.
How similar studies have performed: Other studies have shown promising results with robotic surgical approaches in various oncological settings, suggesting potential for success in this study as well.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age major or equal 18 years * Patients who will undergo radical cystectomy * Consent to participate Exclusion Criteria: * Absence of willingness to participate * Further refusal to participate to the study
Where this trial is running
Florence, Tuscany
- Careggi University Hospital — Florence, Tuscany, Italy (Recruiting)
Study contacts
- Principal investigator: Arcangelo Sebastianelli, MD — Careggi Hospital, University of Florence
- Study coordinator: Simone Morselli, MD
- Email: simone.morselli.89@gmail.com
- Phone: 3473050852
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.