Nurse-Led checkups could catch leukemia drug side effects sooner
NCT ID NCT06082804
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether an advanced practice nurse (APN) can help people with chronic myeloid leukemia (CML) by catching mild side effects early. About 60 adults starting or changing oral therapy will be followed. The goal is to see if nurse-led care improves quality of life, treatment adherence, and how well the leukemia responds, compared to standard doctor-only visits.
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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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2023
- Expected to finish
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Dec 2027
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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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.
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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: * Age ≥ 18 years old. * CML patient in chronic phase, eligible for oral therapy. * Newly diagnosed CML and/or initiating oral therapy : * Patient changing treatment for non-response or loss of therapeutic response or toxicities, on the condition that these toxicities are resolved or grade I maximum at the time of inclusion. * Newly start of oral therapy. * Patient eligible to a follow-up by an advanced practice nurse. * Patient capable to understand french and complete a questionnaire. Exclusion Criteria: * Patient that had a follow-up \> 3 months by an advanced practice nurse for CML before inclusion. * Patient changing treatment for toxicities, if these toxicities are still \> grade I at inclusion. * Patient enrolled in another interventional research protocol for CML. * Pregnant women. * Patient under legal protection, deprived of liberty or unable to be included in a research protocol.
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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 d'Avignon, Hôpital Henri Duffaut
RECRUITINGAvignon, France
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