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Clinical Trial Summary

This is a randomized controlled trial that will be preceded by a safety trial focusing on the safety and efficacy of robotic telesurgery. The hypothesis is that robotic telesurgery has a non-inferior primary endpoint event rate to local laparoscopic surgery.


Clinical Trial Description

First, a safety run-in trial for robotic telesurgery will be conducted and evaluated according to "3+3 design". At least 3 patients of each cancer type (including liver cancer,renal cancer and rectal cancer) will be enrolled for robotic telesurgery. If there is a tumor type for which the prior safety trial is terminated, the subsequent randomized controlled trial will not include patients of that type. Second, after passing the safety run-in trial, a randomized controlled trial will be performed. New patients with each cancer type who met the enrollment criteria will be randomly assigned to either the laparoscopic surgery group(control group) or the robotic telesurgery group (intervention group) (84 patients in each group, 168 patients in total) in a 1:1 two-group parallel design. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06369597
Study type Interventional
Source Sun Yat-sen University
Contact Kuang Ming, PhD
Phone 008687755766
Email kuangm@mail.sysu.edu.cn
Status Not yet recruiting
Phase N/A
Start date April 15, 2024
Completion date March 31, 2025

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