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A study of Coseal surgical sealant for surgery of left ventricular aneurysm.

A study of Coseal surgical sealant for surgery of left ventricular aneurysm.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039339
Enrollment
Unknown
Registered
2020-10-24
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-01-25

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

Conditions

left ventricular aneurysm

Interventions

control group (retrospective):regular hemostasis
experimental group:Coseal for assistant hemostasis

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science And Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for primary coronary artery revascularization with a planned LVA repair or LVA repair by decision during operation.

Exclusion criteria

Exclusion criteria: Patients undergo emergent operation; other concomitant procedure expect coronary artery bypass graft. Underwent cardiac procedure previously.

Design outcomes

Primary

MeasureTime frame
Blood loss at the postoperative day 1 morning;—

Secondary

MeasureTime frame
Blood transfusions volume;the amount of drainage within 48h after surgery;reoperation for bleeding;mediastinitis;30-day mortality;readmissions rate;—

Countries

China

Contacts

Public ContactWei Xiang

Tongji Hospital, Tongji Medical College, Huazhong University of Science And Technology

xiangwee_hust@163.com+86 2783665290

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026