None listed
Conditions
Interventions
Medical Device : In the control group, after completing the skin closure with subcuticular sutures on the deep cutaneous layer and dermis layer, the adhesive is applied. In the experimental group, the
Sponsors
The Catholic University of Korea, St. Vincent's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Aged 19 years and older, up to 85 years Patients undergoing laparoscopic, robotic, or open surgery Patients with a wound length of 4 cm or more American Society Anesthesiologist sscore of 1-3 Eastern Cooperative Oncology Group performance status of 1-2 Individuals who understand the purpose of the study, consent to participate, and allow their participation in the research
Exclusion criteria
Exclusion criteria: Individuals under 18 years of age or over 86 years of age Female patients who are pregnant or planning to become pregnant American Society Anesthesiologist score = 4 Eastern Cooperative Oncology Group performance status = 3 Patients with a history of surgery at the same site where the procedure is being performed Patients with systemic infections immediately prior to surgery or uncontrolled diabetes Patients with hypersensitivity to cyanoacrylate, formaldehyde, or Solvent Violet 13 dye
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound dehiscence rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Rate of wound infection | — |
Countries
Korea, Republic of
Contacts
Public ContactNina Yoo
The Catholic University of Korea, St. Vincent's Hospital
Outcome results
None listed