Which skin glue is gentler? new study puts three to the test
NCT ID NCT05492721
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested three different skin glues (Dermabond, Swiftset, and Liquiband) used to close small incisions after laparoscopic or robotic abdominal surgery. 180 adults each received two different glues on opposite sides of their incisions. The main goal was to see which glue caused less contact dermatitis (redness or rash). The trial is complete, and results will help surgeons choose the gentler option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- skin glue (2-Octylcyanoacrylate and N-butyl-2-cyanoacrylate)
- What this could lead to
- If one glue causes less skin irritation, it could become the preferred choice for closing small surgical cuts, reducing discomfort and rash.
- What could go wrong
- This is a small, completed trial focused on a minor side effect (contact dermatitis). The results may not apply to all surgeries or patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
180 people
The number who actually took part.
- Started
-
Jun 2022
- Finished
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Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18 or older * undergoing an elective laparoscopic or robotic abdominal surgery Exclusion Criteria: * Patients unlikely to follow-up (live out of state, unable to be reached by phone or email) * Patients with a known allergy to 2-Octylcyanoacrylate or N-butyl-2-cyanoacrylate.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Memorial Hermann
Houston, Texas, 77030, United States