Could your phone camera replace blood tests? new study explores
NCT ID NCT05582902
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 60 people with lower-risk myelodysplastic neoplasms (MDS) who need regular red blood cell transfusions. Over 6 months, participants use a smartphone app to answer weekly quality-of-life questions and take photos of their fingernails or eyelids. Researchers aim to see if those photos can help estimate hemoglobin levels, potentially leading to a non-invasive way to monitor anemia.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help develop a smartphone-based tool to estimate hemoglobin levels from photos, potentially reducing the need for blood draws.
- What could go wrong
- This is an observational study, not testing a new treatment. The app-based hemoglobin estimation is exploratory and may not prove accurate enough for clinical use.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2022
- Expected to finish
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Jun 2026
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
Patients suffering from lower-risk myelodysplastic neoplasms (MDS) or MDS/MPN with red blood cell transfusion-dependent anemia
- 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: * Written informed consent * Confirmed diagnosis of lower-risk myelodysplastic neoplasms (MDS; IPSS-R very low, low, intermediate up to 3.5 points) or MDS/MPN overlap including MDS/MPN-RS-T, MDS/MPNu, aCML or non-proliferative chronic myelomonocytic leukemia (CMML) according to World Health Organization (WHO) criteria as determined by microscopic and standard cytogenetic analyses of the bone marrow and peripheral complete blood count (CBC) * Symptomatic transfusion dependent (TD) anemia defined as having received ≥3 units of red blood cells (RBC) within the last 16 weeks prior to screening according to the International Working Group (IWG) criteria for MDS (Platzbecker et al. 2019) Exclusion Criteria: \- Suspected lack of compliance according to the investigator
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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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Charité Universitätsmedizin Berlin
Berlin, 12203, Germany
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Friedrich-Ebert-Krankenhaus GmbH
Neumünster, 24534, Germany
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Gemeinschaftspraxis Hämatologie-Onkologie
Dresden, 01307, Germany
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Klinikum Chemnitz gGmbH
Chemnitz, 09116, Germany
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University Hospital Leipzig
Leipzig, 04103, Germany
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Universitätsklinik Innsbruck
Innsbruck, 6020, Austria
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Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden, 01307, Germany
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Universitätsklinikum Düsseldorf
Düsseldorf, 40225, Germany
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Universitätsklinikum Jena
Jena, 07747, Germany
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Universitätsmedizin Mannheim
Mannheim, 68167, Germany
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Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Mainz, 55131, Germany
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