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A simple rinse during tummy tuck surgery might prevent painful fluid collections
NCT ID NCT07733921
First seen Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time
Summary
This trial tests whether irrigating the surgical site with triamcinolone (a steroid) or hypertonic saline (concentrated salt water) can reduce seroma — a common fluid buildup — after abdominoplasty. Ninety women undergoing tummy tuck surgery are randomly assigned to receive one of the two rinses or no irrigation at all. The goal is to see if either rinse lowers the number of seromas and allows drains to be removed sooner.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- triamcinolone or hypertonic saline irrigated into the surgical site during abdominoplasty
- What this could lead to
- If one of these irrigations works better than no irrigation, it could offer a simple, low-cost way to reduce seromas and shorten drain time after tummy tuck surgery.
- What could go wrong
- This is a small, single-center trial with 90 patients, so results may not apply to everyone. Triamcinolone is a steroid and could increase infection risk or impair wound healing.
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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90 people
The number who actually took part.
- Started
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Nov 2023
- Finished
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Aug 2025
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Females 2. Age: 18-65 3. BMI ≤ 39 4. Pendulous abdomen grades 3 and 4 according to the Matarasso classification of 1991. Exclusion Criteria: 1. Age: \< 18 years and \> 65 years 2. BMI: \>39.1 3. Known allergies to steroidal compounds 4. Uncontrolled medical comorbidities 5. open abdominal surgeries other than caesarian sections. 6. Ventral hernias 7. Ehlers-Danlos and other hyper elasticity syndromes
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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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Faculty of Medicine Cairo University
Cairo, 11956, Egypt
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