HALT Study: Blood Pressure Management in B-cell Cancers on BTKi Treatment
This study, called the HALT Study, is looking at how high blood pressure (hypertension) is managed and how to prevent heart-related problems in people with B-cell cancers like chronic lymphocytic leukemia (CLL) or mantle cell lymphoma (MCL). You could join if you are starting a Bruton tyrosine kinase inhibitor (BTKi) treatment, which is a type of medicine that blocks certain proteins (kinases) in cancer cells. Researchers want to see how often new or worsening high blood pressure occurs and how it affects heart health over 12 months. This is an observational study, meaning you will receive standard care, and researchers will collect information about your health and treatment.
- Study design
- This is an observational study planning to enroll 100 participants. It is not a randomized study, and the phase is not specified.
- What's involved
- You would attend hypertension clinic visits, potentially have optional blood pressure monitoring, electrocardiograms, and impedance cardiography tests. Blood and urine samples would be collected, and your medical records reviewed.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary outcome, major adverse cardiovascular events (MACE), is measured for up to 12 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Evaluation of Hypertension Management and Cardiovascular Adverse Event Prevention in Patients With B-cell Malignancies Undergoing Treatment With Bruton Tyrosine Kinase Inhibitors, the HALT Study
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Joerg Herrmann, MD · PRINCIPAL_INVESTIGATOR · Mayo Clinic in Rochester
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Incidence of major adverse cardiovascular events (MACE)Up to 12 months
1-year MACE rates between patients with B-cell malignancies on BTKi with new or worsening HTN on optimal anti-HTN strategies will be compared with patients who do not develop HTN on BTKi.