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Development of ped UT-Heart

Prospective and interventional research on the development of a multi-scale and multi-physics cardiac simulator "ped UT-Heart" - ped UT-Heart

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052210139
Enrollment
15
Registered
2021-12-22
Start date
2022-03-18
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

Congenital heart disease patients with extremely complex three-dimensional structure of the heart. congenital heart disease

Interventions

To simulate and suggest to surgeons the postoperative hemodynamics of multiple possible surgical techniques based on preoperative cardiac morphology and hemodynamics.

Sponsors

Kurosaki Kenichi
Lead Sponsor
Hisada Toshiaki
Collaborator
PIA Co.,Ltd
Collaborator
Japan Medical Device Corporation
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with pediatric congenital heart disease requiring life-sustaining cardiac repair surgery. (2) Patients under 15 years of age (when consent is obtained from a substitute). (3) Patients who need to undergo cardiac catheterization, cardiovascular angiography, and MSCT angiography to determine the diagnosis and treatment plan. (4) Patients scheduled to undergo surgery for congenital heart disease within 180 days of obtaining consent. (5) Patients with the following congenital heart diseases in which the three-dimensional structure of the heart and great vessels are extremely complicated. 1. Double outlet right ventricle 2. Complete transposition of the great arteries 3. Congenitally corrected transposition of the great arteries 4. Coarctation of aorta/ Interrupted aortic arch 5. Ventricular septal defect with multiple defects 6. Univentricular Heart (including complete atrioventricular septal defect with unbalanced ventricles) 7. Tetralogy of Fallot with or without pulmonary atresia 8. Hypoplastic left heart syndrome and its analogs

Exclusion criteria

Exclusion criteria: (1) Critically ill patients who may require urgent cardiac repair surgery before the simulation using the ped UT-Heart system is available. (2) Patients who are allergic to contrast media used in MSCT and cardiac catheterization/angiography. (3) Patients for whom follow-up until 30 days after surgery is difficult. (4) Patients who are judged by the principal investigator to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Overall postoperative evaluation of the usefulness of ped UT-Heart in assisting in the choice of procedure as assessed by the surgeon (Essential or Very useful on the Likert scale)

Secondary

MeasureTime frame
1. survival rate at 30 days after surgery 2. length of stay in ICU 3. presence and duration of assisted circulation in ICU 4. cardiac arrest time in surgery 5. cardiopulmonary resuscitation time in surgery 6. reoperation or not 7. catheterization or not 8. changes in the results of cross-sectional echocardiography (preoperative and 30-day postoperative comparison) 9. assessment of neurological development at 30 days postoperatively (if performed)

Contacts

Public ContactIsao Shiraishi

National Cerebral and Cardiovascular Center

shiraishi.isao.hp@ncvc.go.jp+81-6-6170-1070

Outcome results

None listed

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