A Study Comparing Skin Adhesive With Staple for Surgical Incision Closure After Laparoscopic / Robotic Bowel Resection
Benign or Malignant Diseases With Indication for Laparoscopic or Robotic Colorectal Resection
About this trial
This is an interventional treatment trial for Benign or Malignant Diseases With Indication for Laparoscopic or Robotic Colorectal Resection
Eligibility Criteria
Inclusion Criteria:
A. 19-year-old or older adults B. elective laparoscopic or robotic colorectal resection C. clean-contaminated surgery without any intraoperative contamination D. The longest incision should be 15cm or shorter E. participant should voluntarily sign inform consent form
Exclusion Criteria:
A. emergency surgery or conversion-to-open surgery B. the longest skin incision longer than 15cm C. intraoperative contamination due to intestinal perforation or any other reason D. ECOG grade 3 or higher E. patients who are not be able to receive surgery within 30 days after screening F. patients who are refused to sign the informed consent form voluntarily
Sites / Locations
- Severance Hospital, Yonsei University Health SystemRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
LSA (liquid skin adhesive)
Stapler
surgical wound closure with liquid skin adhesive (LiquiBand®)
surgical wound closure with stapler