A Study to Validate the Safety and Feasibility of ArtiSential in Colorectal Cancer Surgery Using Prospectively Constructed Multi-center Registry

  • End date
    Dec 31, 2029
  • participants needed
  • sponsor
    Samsung Medical Center
Updated on 24 October 2022
cancer surgery
low anterior resection


This study is to validate the safety and feasibility of ArtiSential (Articulating laparoscopic instrument) colorectal surgery and compare it with robotic surgery for patients with rectal cancer and rectosigmoid junction cancer.

Condition Rectal Cancer, Rectosigmoid Cancer, Rectosigmoid Junction Cancer
Treatment ArtiSential
Clinical Study IdentifierNCT05566249
SponsorSamsung Medical Center
Last Modified on24 October 2022


Yes No Not Sure

Inclusion Criteria

Age : 18 ~ 80 year old male or female
Biopsy-proven adenocarcinoma
Rectal cancer or Rectosigmoid junction cancer
Primary cancer
Non-metastatic cancer
Planned (or elective) curative resection
Low anterior resection with double-stapled technique

Exclusion Criteria

Preoperative systemic chemotherapy
Distant metastasis at initial diagnosis
Palliative surgery
Emergent surgery
Lynch syndrome or FAP-associated cancer
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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