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Robotic mitral valve repair using da Vinci Surgical System for mitral regurgitation: A safety and feasibility study

Robotic mitral valve repair using da Vinci Surgical System for mitral regurgitation: A safety and feasibility study - Robotic mitral valve repair: A safety and feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028160
Enrollment
3
Registered
2017-08-01
Start date
2017-08-01
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

mitral regurgitation (MR)

Interventions

Sponsors

Ministry of Education
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) MR is dianosed. 2) MR which is a operative indication (a) acute MR with symptum (b) chronic MR with NYHA II-IV and LVEF > 30% (c) chronic MR without symptum and LVEF ranging from 30% and 60% or LVDs > 40mm 3) obtained infromed consent 4) the age between 20 years and 80 years

Exclusion criteria

Exclusion criteria: 1) a patient who has a cancer 2) a patient with hemodialysis 3) a patient who participates in other clinical studies 4) a patient who had myocardial infarction within 30 days 5) a patient who had stroke within 180 days 6) a patient who had coronary stent within 30 days 7) a patient who has other procedures than mitral valve, except Maze or PV isolation 8) LVEF > 30% 9) BMI > 35kg/m2 10) active endocarditis 11) a patient who had previously sternotomy or right thoracotomy 12) a patient who had previously radiation therpay on his chest 13) a patient whom the principal investigator considers inappropriate for this clinical study

Design outcomes

Primary

MeasureTime frame
MR after 2 weeks postoperatively MR after 3 months postoperatively

Countries

Japan

Contacts

Public ContactYasushi Yoshikawa

Osaka University Hospital Cardiovascular Surgery

yoshikawa@surg1.med.osaka-u.ac.jp06-6879-3154

Outcome results

None listed

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