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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04765748
Other study ID # 20-031
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 11, 2021
Est. completion date December 27, 2022

Study information

Verified date April 2024
Source RWTH Aachen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Prospecrtive study including 20-30 randomized patients treated by open repair because of an TAAA larger than 55 mm During the surgery, a heart lung machine is applied for distal perfusion during aortic cross clamping to enable distal organ perfusion. Regardless an intensive inflammatory reaction is a well known effect after reperfusion, leading to a uncontrolled inflammation during th first days after surgery. This may be associated to bad outcome and decreased survival rates. By the application of a intraoperative cytokine and DAMP filter this negative ffect could be reduced, resulting in a better outcome after surgery.


Description:

Prospecrtive study including 20-30 randomized patients treated by open repair because of an TAAA larger than 55 mm During the surgery, a heart lung machine is applied for distal perfusion during aortic cross clamping to enable distal organ perfusion. Regardless an intensive inflammatory reaction is a well known effect after reperfusion, leading to a uncontrolled inflammation during th first days after surgery. This may be associated to bad outcome and decreased survival rates. By the application of a intraoperative cytokine and DAMP filter this negative ffect could be reduced, resulting in a better outcome after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 27, 2022
Est. primary completion date November 27, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: Suffering from a TAAA larger than 55mm Exclusion Criteria: immunosupprive therapy pregnancy -

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Cytosorb
Cytokine filter, which can be used intraoperatively while using a heart lung machine

Locations

Country Name City State
Germany Alexander Gombert Aachen NRW

Sponsors (1)

Lead Sponsor Collaborator
RWTH Aachen University

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amount of perioperative catecholamine usage in mg/dl for the first seven days after surgery amount measured in mg/dl 7 days perioperatively -10 day postoperatively
Primary Amount of transfusion required during and after the surgery, assessed in transfusion more or less than 5 blood bags packed cells, erythrocyte concentrate 7 days perioperatively 5-10 day postoperatively
Secondary Acute kidney injury, measured using serum creatinine in mg/dl AKI assessed according to the KDIGO classification perioperatively for the first 7 days after surgery 7 days perioperatively, -10 day postoperatively
Secondary Patients survival for the first 12 months after surgery Survival yes/no within the first 12 months after surgery 12 months 10-14 months postopertaibely
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