New wound closure method tested in High-Risk surgery patients
NCT ID NCT03861065
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at a new way to close surgical wounds in women at high risk for complications after gynecologic abdominal surgery. Instead of leaving the wound partially open to heal, the new method closes it partially right after surgery and fully closes it a few days later. The study aimed to see if this approach leads to fewer infections and better healing, but it was stopped early with only 8 participants.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tertiary wound closure procedure
- What this could lead to
- If successful, this could lead to a better way to close surgical wounds that lowers infection risk and improves healing.
- What could go wrong
- The study was terminated early with only 8 participants, so results are very limited and may not apply to others.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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8 people
The number who actually took part.
- Started
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Feb 2019
- Finished
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Nov 2020
- Lead sponsor
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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
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18 to 65 years
- Sex
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Female participants only
- Healthy volunteers
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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: * Patients with high risk class II, class III, class IV abdominal wounds * Undergoing laparotomy for gynecologic related disorders * Patients undergoing laparotomy for both benign and malignant diagnoses will be included in this study Exclusion Criteria: * Pregnancy * Allergy to triclosan * Patients undergoing HIPEC
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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
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Comprehensive Cancer Center of Wake Forest University
Winston-Salem, North Carolina, 27157, United States
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Other studies related to the condition(s) this trial covers.
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