Could ionized gas help fight breast cancer after surgery?
NCT ID NCT06222788
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This trial tests whether a form of ionized gas, called non-thermal plasma, can be safely applied to the area where a breast tumor was removed during surgery. The goal is to find the highest safe dose and see how well patients tolerate it, while also checking cosmetic effects. Adults with breast cancer scheduled for a lumpectomy may participate, and they will receive a single plasma treatment during their operation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Non-thermal plasma (ionized gas) applied to the tumor bed during surgery
- What this could lead to
- If safe, this approach could offer a new way to treat the area around a removed breast tumor, potentially reducing the chance of cancer returning.
- What could go wrong
- This is an early safety trial with only 30 participants, so it may not prove effective. Risks include potential side effects like infection, skin ulcers, or chest wall damage.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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 years and older
- 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: 1. Age ≥18 years at the time of signing study consent. 2. ECOG ≤2. 3. Patient with T1-4 breast cancer for groups A and B; patient with T1/T2 breast cancer for group C (based on physical exam, not radiological measurements). 4. Patient is scheduled to undergo a lumpectomy. Exclusion Criteria: 1. Prior treatment for the tumor of interest (including chemotherapy, immunotherapy, radiotherapy). 2. Patient planning to or undergoing intraoperative radiotherapy. 3. Diabetes (types I and II). 4. Hypercortisolism. 5. Collagen vascular disease. 6. Patient requiring systemic corticosteroids at physiologic doses exceeding 10 mg/day of prednisone or its equivalent. 7. Patient receiving daily chemotherapy for rheumatological conditions. 8. Pregnancy (a urine pregnancy test must be obtained for non-sterile women of childbearing potential prior to surgery).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Centre Hospitalier de l'Université de Montréal - CHUM
RECRUITINGMontreal, Quebec, h2X0A9, Canada
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