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Multicenter Study of TCD-51073(E) (Feasibility Study)

Multicenter Study of TCD-51073(E) (Feasibility Study) - Feasibility Study of TCD-51073(E)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029824
Enrollment
6
Registered
2017-11-06
Start date
2017-11-06
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

Severe heart failure due to chronic ischemic heart disease

Interventions

Sponsors

Terumo Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients falling under any of the following with regard to the quality of the HeartSheet 1)When it is predicted that skeletal myoblasts do not satisfy the number of transplants assumed 2) In the sheet preparation confirmation test, when deviating from the standing time after sowing the cells (2) Patient with tissue collection using collection / subculture kit of HeartSheet (3) Patients who sign written informed consent prior to the clinical study (4) Patients who are able to undergo all scheduled observations and consent to all details of the observations.

Exclusion criteria

Exclusion criteria: (1) Patients who do not have sheets (2) Patients with a history of hypersensitivity to the components of the investigational product. (3) Patient who can not open-heart surgery. (4) Patients who are judged to be inappropriate for the study by the investigator or the sub investigators.

Design outcomes

Primary

MeasureTime frame
Survival rate(Cardiac disease related death)

Countries

Japan

Contacts

Public Contactkazuo tamada

Terumo Corporation Clinical Development Department

Rinshokenkyu_HS@terumo.co.jp03-6742-8500

Outcome results

None listed

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