RecruitingNot ApplicableNCT05321134

Evaluation of SINGLE PORT (SP) Robotic Technology in Colorectal Surgery


Sponsor

University of California, Davis

Enrollment

25 participants

Start Date

Apr 28, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Currently a multiport robotic surgery platform (Intuitive Xi) is widely available and used for colorectal surgery indications. A Single port platform (Intuitive SP) is FDA approved for Head and Neck and Urology but has not been widely used in colorectal surgery. This study seeks to evaluate the safe and effective use of the SP platform for colorectal surgery indications.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study evaluates the use of single-port robotic surgery technology for colorectal cancer operations, comparing outcomes to traditional multi-port robotic surgery in terms of safety, recovery, and surgical precision. **You may be eligible if...** - You have colorectal cancer requiring surgical resection - You are a candidate for minimally invasive (robotic or laparoscopic) surgery - You are 18 or older - You have given informed consent **You may NOT be eligible if...** - Your cancer requires emergency surgery - You have had multiple prior abdominal surgeries causing significant scarring - You are not a suitable candidate for general anesthesia Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICESingle port robotic colorectal surgical procedure

After screening and counseling, study subjects who wish to participate will undergo the colorectal surgical procedure (determined based on routine standard clinical care) using the alternate Intuitive Da Vinci Single Port SP system rather than the currently used multiport system, (Intuitive Da Vinci Multiport Xi System). Using standardized case report forms, the investigators will track clinical parameters and describe the safety \& quality event rate for SP platform transabdominal and transanal colorectal operations.


Locations(1)

UC Davis Medical Center

Sacramento, California, United States

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NCT05321134


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