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Bloodtranfusions After Aortic Surgery (FIBTEG)

Primary Purpose

Hemorrhage, Thoracic Aneurysm

Status
Terminated
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Haemocomplettan P
Placebo
Sponsored by
St. Antonius Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemorrhage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Elective surgery for thoracic aneurysm

Exclusion Criteria:

  • Prior trombosis or myocardial infarction, congenital coagulation disorder, use of anti-coagulants prior to surgery, prior thoracic surgery, pregnancy, pre-operative fibrinogen concentration <1g/L

Sites / Locations

  • St Antonius hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Haemocomplettan P

NaCl 0.9%

Arm Description

Study patients that receive Haemocomplettan P

Study patients that receive NaCl 0.9%

Outcomes

Primary Outcome Measures

Number of transfused blood products

Secondary Outcome Measures

Blood loss
Re-operation
Mortality

Full Information

First Posted
November 18, 2014
Last Updated
May 8, 2019
Sponsor
St. Antonius Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02299947
Brief Title
Bloodtranfusions After Aortic Surgery
Acronym
FIBTEG
Official Title
Comparison of a Single Dose Fibrinogen With Placebo and the Number of Blood Transfusions After Ascending Aorta Surgery (FIBTEG Study)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Terminated
Why Stopped
Slow inclusion
Study Start Date
August 1, 2014 (Actual)
Primary Completion Date
April 26, 2018 (Actual)
Study Completion Date
April 26, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Antonius Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to answer the following question: Leads a primary coagulation corrected with a single dose of fibrinogen concentrate after ascending aorta-arc reconstruction to a decrease in the number of allogenic blood transfusions, compared to placebo?
Detailed Description
Cardiothoracic surgery (CTC) is associated with blood loss and an increased risk for impaired coagulation by the use of a CBP. Coagulation is a process of primary hemostasis by adhesion of trombocytes and aggregation, followed by secondary coagulation and fibrin formation. During CTC fibrinogen is the first coagulation factor which reaches critical concentration necessary for clotting. Point of Care clotting assay with thromboelastography (TEG) provides qualitative information on coagulation factors and clot strength. Specific coagulation factor correction of impaired clotting improves clot strength and may reduces the number of perioperative allogeneic blood transfusions, resulting in possible reduction of postoperative blood loss and reduction of the risk of re-operation in the short and long term. The hypothesis of this study is that a single dose fibrinogen concentrate immediately after CTC leads to a decrease in the number of allogenic blood transfusions in patients with clinically impaired clotting, verified by TEG.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhage, Thoracic Aneurysm

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Haemocomplettan P
Arm Type
Experimental
Arm Description
Study patients that receive Haemocomplettan P
Arm Title
NaCl 0.9%
Arm Type
Placebo Comparator
Arm Description
Study patients that receive NaCl 0.9%
Intervention Type
Drug
Intervention Name(s)
Haemocomplettan P
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Number of transfused blood products
Time Frame
24 hours after surgery
Secondary Outcome Measure Information:
Title
Blood loss
Time Frame
24 hours after surgery
Title
Re-operation
Time Frame
30 day after surgery
Title
Mortality
Time Frame
30 day mortality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective surgery for thoracic aneurysm Exclusion Criteria: Prior trombosis or myocardial infarction, congenital coagulation disorder, use of anti-coagulants prior to surgery, prior thoracic surgery, pregnancy, pre-operative fibrinogen concentration <1g/L
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Noordzij, PhD
Organizational Affiliation
St. Antonius Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Antonius hospital
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3435 CM
Country
Netherlands

12. IPD Sharing Statement

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Bloodtranfusions After Aortic Surgery

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