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Fibrinogen as an Alternative to FFP in Aortic Surgery.

Primary Purpose

Coagulopathy in Patients Having Thoraco-Abdominal Aneurysm Repair

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Fibrinogen concentrate
Fresh Frozen Plasma
Sponsored by
University of Edinburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coagulopathy in Patients Having Thoraco-Abdominal Aneurysm Repair focused on measuring Thoraco-Abdominal Aneurysm (TAAA), Coagulopathy, Fresh Frozen Plasma, Fibrinogen Concentrate

Eligibility Criteria

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

Inclusion Criteria:

  • Undergoing elective thoracoabdominal aneurysm repair.
  • Over 18 years of age.
  • Able to give written informed consent.

Exclusion Criteria:

  • Previous aortic surgery (re-do surgery).
  • Emergency surgery.
  • Pregnancy.
  • Females of child-bearing age (less than 45 years) not using medically approved method of contraception.
  • Congenital or acquired coagulopathy.
  • Known allergy to study drug.

Sites / Locations

  • The Royal Infirmary of Edinburgh

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Fresh Frozen Plasma

Fibrinogen concentrate

Arm Description

Outcomes

Primary Outcome Measures

Pattern of coagulation disturbance in the conventional treatment (FFP) and fibrinogen concentrate groups.

Secondary Outcome Measures

Proportion of patients in the fibrinogen group in whom FFP transfusion is required during surgery.
Units of FFP transfused - during surgery and up to 24 hours after surgery.
Units of platelets and allogeneic red cells transfused - during surgery and up to 24 hours after surgery.
Blood loss.

Full Information

First Posted
October 13, 2009
Last Updated
January 28, 2017
Sponsor
University of Edinburgh
Collaborators
NHS Lothian, CSL Behring
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1. Study Identification

Unique Protocol Identification Number
NCT00994045
Brief Title
Fibrinogen as an Alternative to FFP in Aortic Surgery.
Official Title
Coagulopathy During Surgery for the Repair of Extent 4 Thoraco-Abdominal Aortic Aneurysms - Feasibility Study of the Use of Fibrinogen Concentrate by Infusion in Place of Fresh Frozen Plasma.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
June 2010 (Actual)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Edinburgh
Collaborators
NHS Lothian, CSL Behring

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Thoracoabdominal aneurysm (TAAA) repair is a major elective vascular operation associated with a large blood loss and potentially life-threatening clotting abnormalities. Theses clotting abnormalities are principally treated using fresh frozen plasma (FFP) (derived from human blood donations), the administration of which carries a number of risks including virus transmission (human immunodeficiency virus (HIV), hepatitis B, hepatitis C) and infection with variant Creutzfeld-Jacob disease (vCJD). FFP is no longer administered to children or high-usage adults in the UK because of the infection risk, and recently it was decided by a UK advisory body that the use of UK-derived FFP should cease. Fibrinogen concentrate is an alternative treatment option to FFP which is thought have less infection risk (purified, heat treated) and has been in licensed use for many years in other European countries. The investigators have been using fibrinogen concentrate recently in their department as an alternative to FFP with encouraging results. 20 patients undergoing elective TAAA repair at The Royal Infirmary of Edinburgh will be randomly allocated to receive standard treatment (FFP) or fibrinogen concentrate as treatment for clotting abnormalities during their surgery. The investigators will take a number of additional blood samples which will provide valuable information about the pattern of clotting abnormalities during this type of operation. The investigators will also record blood loss and the number of allogeneic (derived from human donors) blood components transfused to the patient (red cells, FFP and platelets). Our primary objective is to assess the pattern of coagulation abnormalities in both groups. We will also examine whether the use of fibrinogen concentrate during TAAA repair avoids the need to administer FFP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coagulopathy in Patients Having Thoraco-Abdominal Aneurysm Repair
Keywords
Thoraco-Abdominal Aneurysm (TAAA), Coagulopathy, Fresh Frozen Plasma, Fibrinogen Concentrate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fresh Frozen Plasma
Arm Type
Active Comparator
Arm Title
Fibrinogen concentrate
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Fibrinogen concentrate
Other Intervention Name(s)
Haemocomplettan P, ATC code: B02B B01
Intervention Description
Fibrinogen concentrate will be administered initially at 2 grammes per hour by continuous infusion. This rate will be adjusted in response to the clinical picture and results of point of care coagulation tests. The infusion will be used intra-operatively.
Intervention Type
Biological
Intervention Name(s)
Fresh Frozen Plasma
Primary Outcome Measure Information:
Title
Pattern of coagulation disturbance in the conventional treatment (FFP) and fibrinogen concentrate groups.
Time Frame
Inra-operatively, and up to 24 hours post-operatively.
Secondary Outcome Measure Information:
Title
Proportion of patients in the fibrinogen group in whom FFP transfusion is required during surgery.
Time Frame
Operative period.
Title
Units of FFP transfused - during surgery and up to 24 hours after surgery.
Time Frame
Peri-operative period.
Title
Units of platelets and allogeneic red cells transfused - during surgery and up to 24 hours after surgery.
Time Frame
Peri-operative period.
Title
Blood loss.
Time Frame
Operative period.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing elective thoracoabdominal aneurysm repair. Over 18 years of age. Able to give written informed consent. Exclusion Criteria: Previous aortic surgery (re-do surgery). Emergency surgery. Pregnancy. Females of child-bearing age (less than 45 years) not using medically approved method of contraception. Congenital or acquired coagulopathy. Known allergy to study drug.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alastair Nimmo, MBChB
Organizational Affiliation
NHS Lothian
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Royal Infirmary of Edinburgh
City
Edinburgh
ZIP/Postal Code
EH16 4SA
Country
United Kingdom

12. IPD Sharing Statement

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Fibrinogen as an Alternative to FFP in Aortic Surgery.

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