The Preventive Efficacy of Carvedilol on Cardiac Dysfunction in Duchenne Muscular Dystrophy
Recruitment status was Recruiting
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Duchenne Muscular Dystrophy Cardiomyopathies |
Drug: Carvedilol |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Carvedilol for the Prevention of Minor Cardiac Damage and Cardiac Function in Duchenne Muscular Dystrophy |
- The suppression of minor cardiac damage indicated as elevation of plasma cTnI [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
- Left ventricular function deterioration assessed by echocardiography In-hospital mortality for cardiac dysfunction In-hospital mortality for any cause Overall mortality [ Time Frame: 5 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 60 |
| Study Start Date: | December 2007 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Carvedilol |
Drug: Carvedilol
2.5-5mg/day
Other Name: Artist, Daich-Sankyo Co.Ltd
|
| No Intervention: Control |
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.
Eligibility| Ages Eligible for Study: | 8 Years to 45 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Male patients with Duchenne muscular dystrophy are required to meet the following criteria:
- Aged 8 to 45 years
- Positive plasma cardiac troponin I (0.06ng/mL) at least 4 blood measurement in every 3 month.
- Left ventricular ejection fraction >30% by echocardiography assessment
- Written informed consent
Exclusion Criteria:
Patients with the following conditions will be excluded from the study:
- Left ventricular ejection fraction <30%
- No plasma cTnI elevation
- beta-blocker is already administered without measurement of plasma cTnI
- Contraindication against treatment with β blockers
- Any other serious disease that could potentially complicate the management and follow-up protocols
Contacts and Locations| Contact: Takao Nishizawa, MD,PhD | +81-52-744-2150 | nishizta@med.nagoya-u.ac.jp |
| Contact: Fumihiko Yasuma, MD,PhD | +81-59-378-1321 | yasuma@suzuka.go.jp |
| Japan | |
| Suzuka Hospial | Recruiting |
| Suzuka, Mie, Japan, 513-8501 | |
| Contact: Takao Nishizawa, MD. PhD +81-52-744-2150 nishizta@med.nagoya-u.ac.jp | |
| Contact: Fumihiko Yasuma, MD. PhD +81-593-78-0337 yasuma@suzuka.go.jp | |
| Sub-Investigator: Fumihiko Yasuma, MD, PhD | |
| Sub-Investigator: Toshimitsu Mori, MD | |
| Sub-Investigator: Motoko Sakai, MD, PhD | |
| Sub-Investigator: Satoshi Kuru, MD, PhD | |
| Sub-Investigator: Seigo Kimura, MD | |
| Sub-Investigator: Takuya Tamura, MD | |
| Sub-Investigator: Kentaro Sahashi, MD | |
| Sub-Investigator: Rei Shibata, MD, PhD | |
| Sub-Investigator: Taiki Ohashi, MD | |
| Principal Investigator: | Takao Nishizawa, MD, PhD | Department of Cardiology, Nagoya University Graduate School of Medicine |
More Information
Publications:
| Responsible Party: | Takao Nishizawa, Department of Cardiology, Nagoya Universtiy Graduate School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00606775 History of Changes |
| Other Study ID Numbers: | TN1966220 |
| Study First Received: | January 22, 2008 |
| Last Updated: | February 4, 2008 |
| Health Authority: | Japan: Institutional Review Board |
Keywords provided by Suzuka Hospital:
|
Adrenergic beta-Antagonists Duchenne Muscular Dystrophy Cardiomyopathies Troponin I |
Additional relevant MeSH terms:
|
Muscular Dystrophy, Duchenne Muscular Dystrophies Cardiomyopathies Muscular Disorders, Atrophic Muscular Diseases Musculoskeletal Diseases Neuromuscular Diseases Nervous System Diseases Genetic Diseases, X-Linked Genetic Diseases, Inborn Heart Diseases Cardiovascular Diseases Adrenergic beta-Antagonists |
Carvedilol Adrenergic Antagonists Adrenergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Physiological Effects of Drugs Antihypertensive Agents Cardiovascular Agents Therapeutic Uses Vasodilator Agents Adrenergic alpha-1 Receptor Antagonists Adrenergic alpha-Antagonists |
ClinicalTrials.gov processed this record on May 19, 2013