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Implement of Autologous Skeletal Myoblast Cell Sheet Transplantation for Dilated Cardio myopathy aiming Precision Medicine (Imple ment of Autologous Skeletal Myoblast Cell Sheet Transplantation for Dilated Cardiomyo pathy aiming Precision Medicine)

Implement of Autologous Skeletal Myoblast Cell Sheet Transplantation for Dilated Cardio myopathy aiming Precision Medicine (Imple ment of Autologous Skeletal Myoblast Cell Sheet Transplantation for Dilated Cardiomyo pathy aiming Precision Medicine)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTb050200131
Enrollment
4
Registered
2021-02-09
Start date
2023-01-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

dilated cardiomyopathy

Interventions

Transplantation of the autologous skeletal my oblast cell sheets on the surface of the heart by open-heart surgery

Sponsors

miyagawa shigeru
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Diagnosed with dilated cardiomyopathy 2)Participate in a series of studies including genetic analysis 3)Suffering from heart failure of NYHA class III or IV 4)Worsening heart failure despite receiving maximum medical therapy such as digitalis, diuretic, angiotensin converting enzyme inhibitor, angiotensin II receptor blocker, beta blocker, aldosterone antagonist, and oral inotropic agents 5)16 years of age or older when at the time of informed consent 6)Concerned worsening heart failure despite receiving the standard surgical treatment (left ventricular reconstruction, mitral valve procedure, and so on) and medical treatment over 3 months ago 7)Left ventricular ejection fraction of <=35% in echocardiography at rest from the past 3 months before the informed consent to the enrollment 8)Patients who can consent to participate in this regenerative therapy research in writing by themselves or patients and their guardians can inform consent if they are minor

Exclusion criteria

Exclusion criteria: 1)Having symptoms of musculoskeletal disease 2)Infected with HIV, HBV, HCV, or HTLV-1 3)Cardiogenic shock due to worsening heart failure 4)Having irreversible organ failure other than their hearts 5)Having malignant tumor 6)Pregnant or possibility of pregnant 7)Refusal of transfusion 8)Having past history of drug or alcohol addiction in the past 6 months before the informed consent 9)Allergy of antibiotics or raw material of animal origin such as fetal bovine serum 10)Having severe pulmonary hypertension 11)Participation in another clinical trial(except for the programing device) or intervention in the past 6 months 12)Patients judged inappropriate to participate in this regenerative therapy with any reasons by the principal investigator or subinvestigators

Design outcomes

Primary

MeasureTime frame
Improvement of LV ejection fraction

Secondary

MeasureTime frame
1) LV reverse remodeling 2)exercise tolerability 3)BNP/ NT-proBNP 4)safety 5)NYHA

Countries

Japan

Contacts

Public Contactyoshito ito

Osaka University Hospital

y-ito@surg1.med.osaka-u.ac.jp+81-6-6879-3154

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026