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Randomized controlled clinical study on the efficacy of empagliflozin in preventing and treating myocardial injury associated with hematopoietic stem cell transplantation in children

Randomized Controlled Clinical Study of Empagliflozin in Preventing Cardiac Myocardial Injury Associated with Hematopoietic Stem Cell Transplantation in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126526
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Cardiac Myocardial Injury Associated with Hematopoietic Stem Cell Transplantation in Children

Interventions

Blank group:Blank control
Intervention group:Empagliflozin

Sponsors

West China Second University Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 16 Years

Inclusion criteria

Inclusion criteria: 1.Written informed consent was obtained from study participants and/or legal guardians in accordance with regional or Institutional Review Board (IRB) requirements; 2.Children with indications for hematopoietic stem cell transplantation after discussion by the transplantation team of the Department of Hematology at West China Second University Hospital; 3.Study participants were aged >=2 years and <=16 years;

Exclusion criteria

Exclusion criteria: 1. Previous use of other anti-cardiac remodeling agents such as ACEIs, ARBs, beta-blockers, and MRA; 2.History of hypersensitivity to empagliflozin, enalapril, or any component of the medication; 3.Patients with concomitant other cardiac diseases: such as structural heart disease, cardiomyopathy, valvular heart disease, ischemia sexually transmitted diseases; 4.Cases with incomplete clinical data or poor image quality that cannot be analyzed; 5.Participants who have participated in other clinical studies within the past three months; 6.History of impaired liver function/historic portal hypertension/historic liver cirrhosis/pancreatitis; 7.History of chronic renal impairment/eGFR <30; 8.History of type I diabetes mellitus; 9.Parents failed to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
The overall longitudinal strain of the left ventricle;

Secondary

MeasureTime frame
Myocardial Enzymology;

Countries

China

Contacts

Public ContactGao Ju

West China Second University Hospital, Sichuan University

gaoju651220@126.com+86 131 1185 4621

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026