About this trial
This study looks at a new robotic surgery tool called the Single Port (SP) system. Traditional robotic surgery often uses a Multi-port system. The goal is to see if the SP system is safe and effective for colorectal surgery cases, like treating colorectal cancer and related disorders. Researchers will compare results from surgeries using both systems to find out how well the SP platform works.
The trial's ID number is NCT05321134. This study is not in a specific phase but is a clinical trial looking at a new procedure. It is regulated by the FDA as a medical device, and the trial hopes to include about 25 participants.
Who can join
This trial is open to adults aged 18 and older, both men and women. Participants must have a colorectal surgery need and be in good health. Women must not be pregnant or breastfeeding. Some health issues may prevent participation, and the trial team will confirm eligibility before joining.
Conditions
Colo-rectal Cancer, Rectal Prolapse, Colostomy Stoma, Colorectal Disorders
Age group
Adult, Older adult
The study team makes the final call on eligibility.
What happens in the study
Participants will have colorectal surgery using the Single Port robotic system. This method is new and different from the usual Multi-port system. Everyone in the study will receive the SP treatment, and their progress will be monitored for safety and quality.
Where
This trial is running at 1 location in the United States. It is currently recruiting.
UC Davis Medical Center
Sacramento, California