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Completed

NCT Number: NCT03775070

Simvastatin Therapy in Patients With Dilated Cardiomyopathy.

Dilated cardiomyopathy (DCM) is the most common childhood cardiomyopathy and is associated with significant early morbidity and mortality. About half of patients die or require heart transplantation within 5 years of diagnosis. The medical therapy for DCM with heart failure includes anti-congestive medications and antiplatelet therapy. Those who fail to improve within the first year of diagnosis usually deteriorated even upon aggressive anti-congestive medications. The investigators had conducted precision-medicine-based approach to provide strategic approach as drug repurposing to identify new treatments. The investigators have identified the beneficial effects from a statin, simvastatin, to restore the cardiac contractility. The investigators would further assess the efficacy of simvastatin to improve the cardiac function in patients with DCM.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

National Taiwan University Hospital

Taipei, 100, Taiwan

About this study

Dilated cardiomyopathy (DCM) is the most common childhood cardiomyopathy and is associated with significant early morbidity and mortality. About half of patients die or require heart transplantation within 5 years of diagnosis. The survival advantage from transplantation is limited, particularly in DCM infants.

The medical therapy for DCM with heart failure includes anti-congestive medications and antiplatelet therapy. Those who fail to improve within the first year of diagnosis usually deteriorated even upon aggressive anti-congestive medications. The investigators had conducted precision-medicine-based approach to provide strategic approach as drug repurposing to identify new treatments. The investigators have identified the beneficial effects from a statin, simvastatin, to restore the cardiac contractility in a DCM proband.The initial experience in the proband is promising.

Simvastatin is effective in lowing LDL and cholesterol, thereby to improve the outcome of patients with coronary arterial disease, familiar hypercholesterolemia, etc. For children, though the dosage range and the indication remain unclear, it had been used in children with various diseases. Simvastatin had been given in a small cohort of adult DCM. Patients treated with simvastatin had a lower New York Heart Association functional class compared with those receiving placebo. The LVEF also improved in the simvastatin group. The investigators would further assess the efficacy of simvastatin to improve the cardiac function in patients with DCM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who have already received anti-congestive medications for at least three months and still have compromised LV function (LVEF < 45% and the Z score of the LV end-diastolic diameter > 2.0).
  • Patients who have persistent or even worsening heart failure after one month of anti-congestive medications.
  • Patients who have positive family history of dilated cardiomyopathy and have received anti-congestive medications for one week.

Exclusion criteria

  • Patients who underwent prior cardiac surgery. Those who received DCM related cardiac surgery, such as mitral valve plasty, for longer than a year are not subject to this restriction.
  • Patients who had liver / renal dysfunction.
  • Patients who are pregnant or plan to pregnancy in the period of study.
  • Patients who are intolerance to simvastatin therapy.

Treatment and study plan

simvastatin

Drug
  • Starting dosage: in adult, the dose of simvastatin is 10 mg once daily. In children, the dose is 0.25mg/Kg/day (maximum dose: 10 mg/d).
  • Target dosage: in adult, the dose of simvastatin is 20 mg once daily. In children, the dose is 0.5mg/Kg/day (maximum dose: 20 mg/d).
  • The basic anti-congestive medication will be kept as the same.
  • The dosage may be titrated to a lesser dose by investigators according to the patient's condition.

Primary outcomes

  1. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 1st month(The 1st month follow-up time tolerates a 0.5-month window )

  2. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 3rd month(The 3rd month follow-up time tolerates a 1-month window )

  3. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 6th month(The 6th month follow-up time tolerates a 1-month window )

  4. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 9th month(The 9th month follow-up time tolerates a 1-month window )

  5. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 12th month(The 12th month follow-up time tolerates a 1-month window )

  6. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 15th month(The 15th month follow-up time tolerates a 1-month window )

  7. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 18th month(The 18th month follow-up time tolerates a 1-month window )

  8. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 21st month(The 21th month follow-up time tolerates a 1-month window )

  9. Change from base line in left ventricular ejection fraction and end-diastolic dimention by cardiac ultrasound.

    Time frame: baseline, 24th month(The 24th month follow-up time tolerates a 1-month window )

  10. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 3rd month(The 3rd month follow-up time tolerates a 1-month window )

  11. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 6th month(The 6th month follow-up time tolerates a 1-month window )

  12. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 9th month(The 9th month follow-up time tolerates a 1-month window )

  13. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 12th month(The 12th month follow-up time tolerates a 1-month window )

  14. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 15th month(The 15th month follow-up time tolerates a 1-month window )

  15. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 18th month(The 18th month follow-up time tolerates a 1-month window )

  16. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 21st month(The 21th month follow-up time tolerates a 1-month window )

  17. Change from baseline in N-terminal pro-brain natriuretic peptide level.natriuretic peptide level.

    Time frame: baseline, 24th month(The 24th month follow-up time tolerates a 1-month window )

Secondary outcomes

  1. Number of participants with treatment-related adverse events as assessed by CTCAE v3.0

    Time frame: Up to 24 months

    We will check patient's biochemistry profile including, lipid profile, liver function and renal function. Treatment-related adverse events would be assessed by CTCAE v3.0

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

An Open Label, Single-armed, Exploratory Study of Simvastatin Therapy on the Cardiac Function in Patients With Dilated Cardiomyopathy.

Acronym: SavDCM

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Dec 13, 2018
Registry last updated
Aug 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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