Breath test aims to classify leukaemia in hours, not days
NCT ID NCT07826897
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Doctors often wait days for genetic tests to classify acute myeloid leukaemia (AML) and guide treatment. This trial tests whether breath analysis can detect metabolic products from leukaemia and classify the disease faster. Participants give breath samples and extra blood tests during their first two treatment cycles, coordinated with routine hospital visits. Researchers also collect health information from medical records and questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- breath analysis for volatile organic compounds
- What this could lead to
- If breath analysis works, doctors could classify AML subtypes within hours instead of days, helping them choose the right treatment sooner.
- What could go wrong
- The trial is small and early, so breath signatures may not reliably distinguish AML subtypes or predict treatment response. Breath tests also depend on patients being able to use the mouthpiece, which some cannot.
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.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2029
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.
Who is studied
100 AML patients and 20 autologous-transplant controls
- Ages
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18 years and older
- Sex
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Anyone
- 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: * Diagnosis of an acute myeloid leukaemia and undergoing treatment * OR undergoing autoHSCT for lymphoid/myeloma disease in remission Exclusion Criteria: * inability to perform brath analysis * anatomical barriers preventing use of the mouthpiece.
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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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University Hospital of Zurich
Zurich, Canton of Zurich, 8091, Switzerland
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Other studies related to the condition(s) this trial covers.
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- Can a Chemo-Transplant combo rescue patients whose leukemia resists standard treatment?
- Can a liposomal chemo combo improve outcomes before stem cell transplant?
- Can a new drug regimen beat the standard for stem cell transplant complications?
- Can a targeted pill keep leukemia from returning after transplant?