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Dilutional Coagulopathy in Patients Undergoing Elective Surgery

Primary Purpose

Blood Coagulation Disorder

Status
Completed
Phase
Phase 1
Locations
Denmark
Study Type
Interventional
Intervention
Fibrinogen
Sponsored by
Christian Fenger-Eriksen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Blood Coagulation Disorder focused on measuring Blood coagulation disorder, acquired, Hemodilution, Fibrinogen, Hemostasis, HES

Eligibility Criteria

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

Inclusion Criteria:

  • > 18 years
  • Indication for performing cystectomia
  • Written informed consent

Exclusion Criteria:

  • Uses of acetyl-salicylic or non-steroid anti-inflammatory drugs 2 days prior to blood sampling.
  • Abnormal preoperative coagulations parameters (Platelets, PP, APTT, D- dimer, Fibrinogen, AT, TT)
  • Disseminated cancer and/or bone metastasis
  • Medical history of ischemic heart disease, claudicatio, or arteriosclerosis
  • Medical history of previous thrombo-embolic event
  • Renal failure defined as clinical relevant abnormal levels of creatinine
  • Liver failure defined as clinical relevant abnormal levels of ALAT
  • Hypersensibility to Voluven, Haemocomplettan or ingredients
  • Fertile women not using safe contraception

Sites / Locations

  • Aarhus University Hospital, Department of Anaesthesiology

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Fibrinogen

Arm Description

Nacl

Fibrinogen

Outcomes

Primary Outcome Measures

Dynamic whole blood clot formation.

Secondary Outcome Measures

A) Single coagulation factor activities B) Platelet function C) Whole blood clot stability. D) Thrombin generation.

Full Information

First Posted
June 27, 2007
Last Updated
November 30, 2015
Sponsor
Christian Fenger-Eriksen
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1. Study Identification

Unique Protocol Identification Number
NCT00493272
Brief Title
Dilutional Coagulopathy in Patients Undergoing Elective Surgery
Official Title
Fibrinogen vs Placebo for Improvement of Clot Strength
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Christian Fenger-Eriksen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the present study is to perform a comprehensive description of haemostasis parameters before and after haemodilution with Hydroxyethyl starch (HES) following acute bleeding during elective surgery. Moreover the study aims to test the in vivo haemostatic potential of fibrinogen concentrate in dilutional coagulopathy caused by HES in a clinical, prospective, placebo-controlled randomised setup. We hypothesise; a) A coagulopathy is induced following in vivo haemodilution; b) the coagulopathy is improved or partially improved by fibrinogen.
Detailed Description
Background Hydroxyethyl starch (HES) is a group of artificial colloid solutions widely used for plasma expansion and volume resuscitation. HES consist of branched chains of hydroxylated glucose molecules defined by average molecular weight, degree of hydroxyethylation, and C2/C6 ratio. Several clinical reports and in vitro experiments have documented an impaired coagulation system induced by haemodilution with HES and other colloid plasma expanders. The exact mechanisms responsible for HES induced coagulopahty are not fully understood although reduced levels of von Willebrand factor (vWF), acquired platelet dysfunction, reduced factor VIII levels, and dysfunctional fibrinogen polymerization seems to reflect an important aspect of the pathogenesis. Experimental laboratory studies performed in our centre and verified by several other research groups have shown successful reversal of the colloid plasma expander induced coagulopathy by fibrinogen concentrate.10-13 So far, the present knowledge are based on laboratory experiments and animal studies. Hence, it appears desirable to perform a comprehensive description of haemostasis parameters following HES induced dilutional coagulopathy in an acute clinical bleeding situation. Materials and Methods Study design: Clinical, prospective, double-blind, randomised, place-controlled trial. Blood samples: Primary end point: Dynamic whole blood clot formation Secondary end points: A) Single coagulation factor activities B) Platelet function C) Whole blood clot stability. D) Thrombin generation Perspectives: Serious surgical and traumatic bleedings are common and associated with a high mortality rate. The present study can significantly contribute to our overall understanding of the mechanisms involved in HES induced dilutional coagulopathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood Coagulation Disorder
Keywords
Blood coagulation disorder, acquired, Hemodilution, Fibrinogen, Hemostasis, HES

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Nacl
Arm Title
Fibrinogen
Arm Type
Active Comparator
Arm Description
Fibrinogen
Intervention Type
Drug
Intervention Name(s)
Fibrinogen
Other Intervention Name(s)
Active drug
Intervention Description
Fibrinogen behandling
Primary Outcome Measure Information:
Title
Dynamic whole blood clot formation.
Time Frame
60 minutes
Secondary Outcome Measure Information:
Title
A) Single coagulation factor activities B) Platelet function C) Whole blood clot stability. D) Thrombin generation.
Time Frame
60 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 18 years Indication for performing cystectomia Written informed consent Exclusion Criteria: Uses of acetyl-salicylic or non-steroid anti-inflammatory drugs 2 days prior to blood sampling. Abnormal preoperative coagulations parameters (Platelets, PP, APTT, D- dimer, Fibrinogen, AT, TT) Disseminated cancer and/or bone metastasis Medical history of ischemic heart disease, claudicatio, or arteriosclerosis Medical history of previous thrombo-embolic event Renal failure defined as clinical relevant abnormal levels of creatinine Liver failure defined as clinical relevant abnormal levels of ALAT Hypersensibility to Voluven, Haemocomplettan or ingredients Fertile women not using safe contraception
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Else Tønnesen, MD, Prof
Organizational Affiliation
Aarhus University Hospital, Department of Anaesthesiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital, Department of Anaesthesiology
City
DK-8200 Aarhus N
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
9806670
Citation
Jamnicki M, Zollinger A, Seifert B, Popovic D, Pasch T, Spahn DR. Compromised blood coagulation: an in vitro comparison of hydroxyethyl starch 130/0.4 and hydroxyethyl starch 200/0.5 using thrombelastography. Anesth Analg. 1998 Nov;87(5):989-93. doi: 10.1097/00000539-199811000-00002.
Results Reference
background
PubMed Identifier
2442613
Citation
Damon L, Adams M, Stricker RB, Ries C. Intracranial bleeding during treatment with hydroxyethyl starch. N Engl J Med. 1987 Oct 8;317(15):964-5. doi: 10.1056/NEJM198710083171517. No abstract available.
Results Reference
background
PubMed Identifier
9024047
Citation
Baldassarre S, Vincent JL. Coagulopathy induced by hydroxyethyl starch. Anesth Analg. 1997 Feb;84(2):451-3. doi: 10.1097/00000539-199702000-00040. No abstract available.
Results Reference
background
PubMed Identifier
11810130
Citation
de Jonge E, Levi M, Buller HR, Berends F, Kesecioglu J. Decreased circulating levels of von Willebrand factor after intravenous administration of a rapidly degradable hydroxyethyl starch (HES 200/0.5/6) in healthy human subjects. Intensive Care Med. 2001 Nov;27(11):1825-9. doi: 10.1007/s001340101107. Epub 2001 Sep 26.
Results Reference
background
PubMed Identifier
15608046
Citation
Fenger-Eriksen C, Anker-Moller E, Heslop J, Ingerslev J, Sorensen B. Thrombelastographic whole blood clot formation after ex vivo addition of plasma substitutes: improvements of the induced coagulopathy with fibrinogen concentrate. Br J Anaesth. 2005 Mar;94(3):324-9. doi: 10.1093/bja/aei052. Epub 2004 Dec 17.
Results Reference
background
PubMed Identifier
16879481
Citation
Fenger-Eriksen C, Ingerslev J, Sorensen B. Coagulopathy induced by colloid plasma expanders--search for an efficacious haemostatic intervention. Acta Anaesthesiol Scand. 2006 Aug;50(7):899-900. doi: 10.1111/j.1399-6576.2006.01054.x. No abstract available.
Results Reference
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Dilutional Coagulopathy in Patients Undergoing Elective Surgery

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