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The Preventive Efficacy of Carvedilol on Cardiac Dysfunction in Duchenne Muscular Dystrophy

Carvedilol for the Prevention of Minor Cardiac Damage and Cardiac Function in Duchenne Muscular Dystrophy

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00606775
Enrollment
60
Registered
2008-02-05
Start date
2007-12-31
Completion date
2012-12-31
Last updated
2008-02-05

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

Conditions

Cardiomyopathies, Duchenne Muscular Dystrophy

Keywords

Adrenergic beta-Antagonists, Duchenne Muscular Dystrophy, Cardiomyopathies, Troponin I

Brief summary

Purpose This cardiac dysfunction in patients with Duchenne muscular dystrophy is associated with minor cardiac damage as indicated by elevation of plasma cardiac troponin I (cTnI). The purpose of this study is to investigate whether the administration of Carvedilol can suppress the minor cardiac damage and prevent deterioration of cardiac function.

Detailed description

The life span in patients with Duchenne muscular dystrophy has been extending due to the development of artificial respiratory devices. According to that, the ratio of cardiac dysfunction as a cause of death has been increasing. This cardiac dysfunction was associated with minor cardiac damage as indicated by elevation of plasma cardiac troponin I (cTnI). Furthermore, and the detection rate of cTnI plasma as revealed to be correlated with the deterioration speed of LV dysfunction assessed by serial echocardiography measurements. Accordingly, if this minor cardiac damage is suppressed, it is postulated that the progression of cardiac dysfunction can be stopped. In the cases with ventricular arrhythmia and tachycardia, we found plasma cTnI became undetectable after administration of beta-blocker. Accordingly, we investigate whether administration of beta-blocker, carvedilol can persistently suppress the minor cardiac damage and lead to suppress the deterioration of LV function. Note that his study preventive study for preserved to moderate LV dysfunction and is not intended to the beta-blocker treatment for severe LV dysfunction. Because we assume that the mechanism of elevation of cTnI is different; spontaneous in preserved to mild LV dysfunction in patients but LV wall stress in severe LV dysfunction in patients with Duchenne muscular dystrophy.

Interventions

DRUGCarvedilol

2.5-5mg/day

Sponsors

Nagoya University
CollaboratorOTHER
Suzuka Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
8 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Male patients with Duchenne muscular dystrophy are required to meet the following criteria: 1. Aged 8 to 45 years 2. Positive plasma cardiac troponin I (0.06ng/mL) at least 4 blood measurement in every 3 month. 3. Left ventricular ejection fraction \>30% by echocardiography assessment 4. Written informed consent

Exclusion criteria

Patients with the following conditions will be excluded from the study: 1. Left ventricular ejection fraction \<30% 2. No plasma cTnI elevation 3. beta-blocker is already administered without measurement of plasma cTnI 4. Contraindication against treatment with β blockers 5. Any other serious disease that could potentially complicate the management and follow-up protocols

Design outcomes

Primary

MeasureTime frame
The suppression of minor cardiac damage indicated as elevation of plasma cTnI2 years

Secondary

MeasureTime frame
Left ventricular function deterioration assessed by echocardiography In-hospital mortality for cardiac dysfunction In-hospital mortality for any cause Overall mortality5 years

Countries

Japan

Contacts

Primary ContactTakao Nishizawa, MD,PhD
nishizta@med.nagoya-u.ac.jp+81-52-744-2150
Backup ContactFumihiko Yasuma, MD,PhD
yasuma@suzuka.go.jp+81-59-378-1321

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026