Open-laber observation, prospective, controlled, randomized clinical trial for the Coseal surgical sealant in Bentall procedures±SUN 'S Procedures

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1800019327

Enrollment

Unknown

Registered

2018-11-06

Start date

2018-11-15

Completion date

Unknown

Last updated

2018-11-19

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

Conditions

Aortic dissection

Interventions

Group 1:Intraoperative administration of chemical agents in the experimental group

Group 2:The control group did not give or give placebo.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with cardiovascular diseases undergoing Bentall procedures±Suns procedure; 2. Stcrnotomy/Tacotomy.

Exclusion criteria

Exclusion criteria: 1. Patients known hypersensitivity to the components of the investigational products; 2. Patients with contraindications for use of Coseal; 3. Patients known Immune system disorders, immunodeficiency; 4. Patients concurrently participating in another clinical trial and having received another investigation drug or device within the last 30 days; 5. Patients receiving any other surgical glue-during the surgical procedure; 6. Patients reoperation; 7. Patients with known or suspected preoperative coagulation disorder.

Design outcomes

Primary

Measure	Time frame
Intraoperative blood loss;	—

Countries

China

Contacts

Public ContactXiaolong WANG

Beijing Anzhen Hospital affiliated to Capital Medical University

Wangxiaolong1971@hotmail.com+86 13801233478

Outcome results

None listed

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