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Clinical Study for Autologous Plateletpheresis in Aortic Dissection Surgery with Cardiopulmonary Bypass

Clinical Study for Autologous Plateletpheresis in Aortic Dissection Surgery with Cardiopulmonary Bypass

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030110
Enrollment
Unknown
Registered
2020-02-23
Start date
2016-12-01
Completion date
Unknown
Last updated
2020-02-25

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

Conditions

Aortic Dissection

Interventions

Case series:autologous platelet separation versus

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patients voluntarily signed the informed consent form of the trial, with good compliance and follow-up; 2. The patients with diagnosis of aortic dissection who undergoing aortic dissection surgery cardiopulmonary bypass; 3. Male and female patients aged 18-75 years and whose weight is more than 50kg; 4. Before the operation, the number of platelets in patients was not lower than the normal range, and the hematocrit (HCT) was more than 35%.

Exclusion criteria

Exclusion criteria: 1. Those who refuse to sign informed consent. 2. Patients with platelet count less than 50x10^9/L, hypoproteinemia and coagulation mechanism disorders; 3. Patients with platelet disease before operation and those who are not suitable for collection during emergency operation; 4. Systemic bacteremia and sepsis; 5. Aspirin, clopidogrel and other antiplatelet drugs were used within 72 hours.

Design outcomes

Primary

MeasureTime frame
perioperative autologous and allogeneic blood transfusion volume;Changes of hemoglobin, platelet count, prothrombin time, APTT and thromboelastogram in perioperative period;postoperative drainage, complications, ICU stay time,hospital mortality, 3-year survival rate, length of hospitalization, Cost of transfusion and hospitalization;perioperative indicators;

Secondary

MeasureTime frame
general condition of patients;

Countries

China

Contacts

Public ContactXianjun Ma

Qilu Hospital of Shandong University

18560087567@163.com+86 18560087567

Outcome results

None listed

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