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Clinical Trial Summary

The objective of the study is to assess the safety and technical feasibility of a new imaging system, used during colorectal resection surgery, named Trident in version 1.0, which could be used by the surgeon during colorectal procedures to obtain information on intestinal tissue oxygenation.


Clinical Trial Description

This is a prospective, non-randomized, single center, feasibility trial. All consecutive patients that fulfil the inclusion/exclusion criteria will be informed about the possibility to be included in the present clinical investigation. Only subjects that have signed the study informed consent will be included in the study. The Trident System v1.0 will be used only during approximately 2 to 5 minutes during a precise surgical step, i.e., just before the final resection of the surgical specimen. Patients will be prospectively followed at 30 days post-surgery. Data will be collected prospectively from the medical records. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05973227
Study type Interventional
Source Intuitive Surgical
Contact Marie Allouis
Phone +33 786 480 495
Email EU Clinical Affairs <DL-Department-ClinicalAffairs-EMEA@intusurg.com>
Status Recruiting
Phase N/A
Start date July 6, 2023
Completion date July 2024