A multicenter randomized controlled trial comparing subcuticular closure versus no subcuticular closure in colorectal cancer surgery for the prevention of surgical site infection (SCISSOR Trial)

未提供0 个研究点目标入组 2,000 人开始时间: 待定

适应症

试验速览

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•Patients aged >=18 years with colorectal cancer who are scheduled to undergo laparoscopic or robot-assisted resection (with a mini-laparotomy via a midline or Pfannenstiel incision).
•Patients in whom wound closure can be performed according to the study protocol.
•Patients who have received a full explanation of the study and have provided written informed consent.

•Patients diagnosed with colorectal cancer accompanied by bowel obstruction who are judged to require emergency or urgent surgery, those requiring preoperative colonic stent placement, or those considered unsuitable for standard mechanical bowel preparation.
•Patients scheduled for placement of prosthetic material (e.g., immediate mesh implantation) at the same incision site.
•Patients with severe active infection or immunocompromised conditions (e.g., severe neutropenia).
•Pregnant women or those with a high possibility of pregnancy.
•Patients in whom standardization of the study procedures is considered difficult (e.g., inability to adhere to the protocol in emergency surgery).
•Patients judged to be inappropriate for inclusion in the study by the principal investigator.

发起方

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