Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Management of Chronic Myeloid Leukemia by Advanced Practice Nurses

Official title: Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia

Run by Centre Hospitalier Henri Duffaut - Avignon · NCT06082804 · Data updated 2026-11-12

This study is testing how Advanced Practice Nurses can help people with Chronic Myeloid Leukemia manage their treatment and improve their quality of life.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorCentre Hospitalier Henri Duffaut - Avignon
Academic / other
Locations1 site (Avignon)
StatusRecruiting
StartedNovember 29, 2023
Main results expectedJune 2027
Study endsDecember 2027
Registry record updatedMarch 4, 2026
Trial IDNCT06082804 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older with chronic phase CML who are eligible for oral therapy.

Probably not a fit

Patients with unresolved grade II or higher toxicities at the time of inclusion may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the role of Advanced Practice Nurses (APNs) in managing patients with Chronic Myeloid Leukemia (CML) during the chronic phase. It focuses on optimizing treatment by addressing adverse events, ensuring treatment compliance, and assessing the quality of life of patients. The study aims to improve early detection of adverse events, which are often underreported, thereby enhancing patient care and therapeutic outcomes. Participants will receive both medical management and follow-up care from APNs.

Why it matters

Potential benefit: If successful, this approach could lead to improved management of CML and better quality of life for patients.

How similar studies have gone: Other studies have shown promising results with APN-led management in chronic conditions, indicating potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Centre Hospitalier d'Avignon, Hôpital Henri Duffaut
    Avignon, France
    Recruiting

Study contacts

  • Principal investigator: Christine Tosello, APN — Centre Hospitalier d'Avignon, Service d'Oncologie Médicale-Hématologie Clinique
  • Study coordinator: Marilyne Grinand, PhD
  • Email: grinand.marilyne@ch-avignon.fr
  • Phone: (+33)432759392

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.