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Investigation of the effect of carvedilol on cardiac function in patients with chronic myeloid leukemia treated with nilotinib and dasatinib

Investigation of the effect of carvedilol on cardiac function in patients with chronic myeloid leukemia treated with nilotinib and dasatinib in Sari city

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241013063353N1
Enrollment
30
Registered
2025-12-29
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic myeloid leukemia. Chronic myeloid leukemia, BCR/ABL-positive

Interventions

Intervention 1: Intervention group: Chronic myeloid leukemia patients treated with nilotinib and dasatinib undergoing carvedilol intervention. Intervention 2: Control group: Chronic myeloid leukemia p

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with chronic myeloid leukemia treated with nilotinib and dasatinib for at least one year Age>18 Sinus rhythm of the heart

Exclusion criteria

Exclusion criteria: Acute and Chronic Heart Failure Low Ejection Fraction History of valvular heart disease or congenital heart disease Systolic blood pressure <90 mm Hg or diastolic blood pressure <60 mm Hg PR interval = 240 ms AV block grade 2-3 History of Asthema Chronic Obsteractive Pulmonary Disease Previous medical history of cardioprotective drugs (such as ACE inhibitors or dexrazoxane) Previous diagnosis of cardiomyopathy, history of coronary artery disease, moderate to severe mitral and aortic disease, and atrial fibrillation. Lack of consent to participate in the study

Design outcomes

Primary

MeasureTime frame
Study of the effect of carvedilol on cardiac function in patients with chronic myeloid leukemia treated with nilotinib and dasatinib in Sari city. Timepoint: Outcomes are measured at 0, 6, and 12 months. Method of measurement: Based on echocardiography by an echocardiogram specialist and measurement of cardiac-specific biomarkers ProBNP, Troponin I.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Bazram

Mazandaran University of Medical Sciences

ali_next@yahoo.com+98 11 4204 0905

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026