Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in Left-sided Colon, Sigmoid, and Rectal Resections

The purpose of this study is to evaluate the safety and performance of the Signia™ power handle, Signia™ circular adapter, and Signia™ Tri-Staple™ 2.0 circular reloads (hereafter referred to as Signia™ circular stapler) in patients undergoing left sided colon, sigmoid, or rectal resections in a post market setting.

Trial Details

NCT ID
NCT07351071
Phase
NA
Sponsor
Medtronic - MITG
Status
RECRUITING
Cancer Type
Colon Cancer Colorectal Cancer
Interventions
  • Signia™ circular stapler with Tri-Staple™ Technology (Signia™ Circular Stapling system)
Locations (sample)
  • New Haven, Connecticut, United States|41.30815,-72.92816
  • Tampa, Florida, United States|27.94752,-82.45843
  • Boston, Massachusetts, United States|42.35843,-71.05977
  • Durham, North Carolina, United States|35.99403,-78.89862
  • Columbus, Ohio, United States|39.96118,-82.99879

Key Eligibility Criteria

  • Subject is competent and willing to provide documented informed consent to participate in this clinical study
  • Subject is intended to undergo an elective left sided colon/colorectal procedure where a creation of an anastomosis will be completed with the Sign…
  • Subject is ≥ 18 years of age at time of consent
  • Preoperative Exclusion Criteria:

For full eligibility, visit ClinicalTrials.gov.

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