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NCT Number: NCT07826897

Real-Time Breath Analysis in Acute Myeloid Leukaemia for a Rapid Characterisation of Biological Subtypes and to Predict Therapy Responses

Patients with acute myeloid leukaemia (AML) respond to treatment to differing degrees, owing to the biological diversity of the disease. The diagnostic tests currently available for identifying genetic alterations and selecting the best possible treatment usually take several days before a result is obtained. In our study, the investigators aim to determine whether breath analysis can detect metabolic products of the leukaemia that allow the disease to be classified rapidly.

Participants will undergo additional blood tests and a breath analysis during their routine appointments. This will take place only during the 1st and 2nd treatment cycles. They will also be asked to complete a questionnaire about their state of health. In addition, the study team will collect further information on their state of health (type of leukaemia, type of treatment, other medications, vital signs) from their medical records.

In total, participants will complete 4 such measurements before and during their treatment. The measurements will be coordinated with their outpatient appointments. No assessments will be carried out unless the participants are at the hospital in any case, and they will not have to attend the hospital more often because of their participation in this study.

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Key information

Conditions

AML

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Zurich

Zurich, Canton of Zurich, 8091, Switzerland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. A breath metabolite signature representing AML disease burden

    Time frame: 8 weeks

    A breath metabolite signature representing AML disease burden, and might represent novel AML subtypes or describe cancer metabolic status.

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Sponsors and collaborators

Lead sponsor

Jeremy Deuel

Other

Collaborators

  • ETH Zurich
  • University Hospital, Zürich

Registry information

Official study title

Exhalomics for Phenotyping and Real-Time Stratification in Acute Myeloid Leukaemia (EXHALE)

Acronym: EXHALE

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Sep 17, 2026
Registry last updated
Sep 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.