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Modified Bentall procedure to prevent anastomosis from bleeding

Modified Bentall procedure to prevent anastomosis from bleeding

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014640
Enrollment
Unknown
Registered
2018-01-25
Start date
2018-02-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

The diseases of aortic root including aneurysmal aortic root and aortic dissection

Interventions

study group:Modified Bentall
control group:Bentall with wrapping Group

Sponsors

Wuhan Asia Heart Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 80 Years

Inclusion criteria

Inclusion criteria: Isolated Bentall Procedure

Exclusion criteria

Exclusion criteria: 1. Patients with dissection of the aortic arch, thoracic aorta or abdomino-thoracic aorta; 2. Paitents with other procedures, such as mitral valve surgery, CABG or circulatory arrest, etc.; 3. Paitents with a normal haemoglobin level or hereditary coagulopathies or other severe organic disease.

Design outcomes

Primary

MeasureTime frame
Blood-product consumption including fresh frozen plasma, platelets and red blood cells.;The total postoperative drainage amount including the 1st postoperative day and the 2nd day;

Secondary

MeasureTime frame
CPB time;Cross-Clamp time;Mortality and morbidity;Re-exploration for bleeding;Pulmonary complication;Intensive Care Unit stay;Hospital stay;Renal failure;Neurologic complications including transient deficits and stroke;

Countries

China

Contacts

Public ContactJun Fu

Wuhan Asia Heart Disease Hospital

fujunsir@qq.com+86 027 65796713

Outcome results

None listed

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