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Evaluate early cardiac injury after hematopoietic stem cell transplantation by echocardiography- a single center prospective clinical study

Evaluate early cardiac injury after hematopoietic stem cell transplantation by echocardiography- a single center prospective clinical study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099269
Enrollment
Unknown
Registered
2025-03-20
Start date
2024-01-09
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Cardiomyopathies

Interventions

Mitoxantrone Group:NA
Alkylating agents and antimetabolizers Group:NA
Control Group:NA

Sponsors

Huadong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. patients with hematological malignancies undergoing autologous or allogeneic hematopoietic stem cell transplantation; 2. Patients with hematological malignancies receiving conventional chemotherapy; 3. aged 18-60 years old; 4. Liver and renal function: serum bilirubin <=35µmol/L, AST/ALT < 2 times of the upper limit of normal, blood muscle liver <=150µmol/L; 5. normal cardiac function; 6. physical status score 0-2 (ECOG score); 7. Informed consent was obtained from patients or their family members;

Exclusion criteria

Exclusion criteria: 1. obvious contraindications to chemotherapy drugs; 2. abnormal liver and kidney function beyond the inclusion criteria; 3. severe heart disease, including myocardial infarction and cardiac insufficiency; 4. concurrent malignant tumors of other organs; 5. active TB patients and HIV positive patients; 6. patients with other hematological diseases; 7. pregnant or lactating women; 8. cannot understand or adhere to the study protocol; 9. previous history of intolerance or allergy to drugs in the same class; 10. Co-participating with other clinical investigators; 11. any other circumstances that may prevent the conduct of the study.

Design outcomes

Primary

MeasureTime frame
myocardial enzyme;brain natriuretic peptide, BNP;Endocardial longitudinal strain;Circumferential strain of endocardium;Endocardial strain;cardiac efficiency;

Secondary

MeasureTime frame
Incidence of Heart Failure;Overall survival;safety;

Countries

China

Contacts

Public ContactLynn

Huadong Hospital

cl_point@126.com+86 21 62483180

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026