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Can a carboxy gel prevent wound breakdown after breast reduction?

NCT ID NCT07408960

Symptom relief Sponsor: University of Calgary Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This small pilot study will test whether a special gel called CO2Lift can reduce wound breakdown after breast reduction surgery. Ten women will have the gel applied to one breast and a placebo to the other, and researchers will track healing for 12 weeks. The main goal is to see if a larger study is possible, but they will also check if the gel improves wound healing and tissue oxygen levels.

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

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

About 10 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

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 to 85 years

Sex

Female participants only

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Female patients aged 18 to 85 years * Undergoing bilateral reduction mammoplasty using an inverted-T (Wise pattern) technique * American Society of Anesthesiologists (ASA) physical status classification I-III * Able and willing to provide informed consent * Willing and able to comply with study procedures and follow-up visits Exclusion Criteria: * Prior radiation therapy to either breast * Prior breast reduction surgery to either breast * Known allergy or sensitivity to CO2Lift®, Vaseline®, or any of the ingredients * Pregnant or breastfeeding * History of immunosuppressive therapy * History of keloid formation * Active local or systemic infection at the time of surgery * Current smoker or history of substance abuse (including alcohol or illicit drugs) * Use of asymmetrical breast reduction techniques * Anticipated inability to complete follow-up or loss to follow-up

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Conditions

The condition(s) this trial relates to.

Surgical Wound Surgical Wound Dehiscence

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breast reduction Breast surgery Surgical wound Wound breakdown

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

More trials for these conditions

Other studies related to the condition(s) this trial covers.