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Safety and Efficacy of the Use of Regional Anticoagulation With Citrate in Continuous Venovenous Hemofiltration

Primary Purpose

Kidney Failure, Acute

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
trisodium citrate
nadroparin
Sponsored by
Onze Lieve Vrouwe Gasthuis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Failure, Acute focused on measuring kidney failure, acute, venovenous hemofiltration, hemorrhage, heparin, low-molecular-weight, nadroparin, citrates

Eligibility Criteria

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

Inclusion Criteria: Intensive care patients scheduled for continuous venovenous hemofiltration Exclusion Criteria: Severe pre-existent liver failure (cirrhosis Child C), acute liver dysfunction as occurring with septic shock is not a reason for exclusion Active bleeding or bleeding necessitating the infusion of two red blood cell units within 24 hours before starting hemofiltration or a fall in hemoglobin of > 0.5 mmol/l. A fall in hemoglobin/hematocrit as a result of fluid loading is not regarded as bleeding. Surgery within 24 h prior to CVVH. Patients needing full systemic anticoagulation (unfractionated heparin in a dose of > 10000 IU/day, or nadroparin > 3800 IU/day) for other reasons Expectation to die within 24 hours Chronic dialysis Proven or suspected heparin-induced thrombocytopenia

Sites / Locations

  • Onze Lieve Vrouwe Gasthuis

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

citrate

nadroparin

Arm Description

regional anticoagulation with citrate

nadroparin is a low molecular weight heparin

Outcomes

Primary Outcome Measures

bleeding complications
transfusion requirement
filter survival

Secondary Outcome Measures

mortality

Full Information

First Posted
February 1, 2006
Last Updated
August 25, 2009
Sponsor
Onze Lieve Vrouwe Gasthuis
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1. Study Identification

Unique Protocol Identification Number
NCT00286273
Brief Title
Safety and Efficacy of the Use of Regional Anticoagulation With Citrate in Continuous Venovenous Hemofiltration
Official Title
Safety and Efficacy of the Use of Regional Anticoagulation With Citrate in Continuous Venovenous Hemofiltration, a Randomized Controlled Trial Comparing Anticoagulation With Citrate to the Low Molecular Weight Heparin Nadroparin
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Completed
Study Start Date
March 2003 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
March 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Onze Lieve Vrouwe Gasthuis

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Severely ill patients admitted to the intensive care unit may develop an acute failure of kidney function. To bridge the period to recovery, renal function is temporarily replaced by continuous venovenous hemofiltration (CVVH). To prevent clotting of the hemofiltration circuit, heparin is generally used, providing anticoagulation in the circuit and the patient. As a result, bleeding complications may occur, necessitating the transfusion of blood. Anticoagulation of the circuit can also be obtained with the use of tri-sodium citrate, which provides anticoagulation of the circuit without affecting coagulation in the patient and thus without increasing his/her risk of bleeding. The use of citrate may however cause metabolic complications. Primary aim of the present study is to show in a larger group of intensive care patients whether the use of regional anticoagulation with citrate is safe compared to systemic anticoagulation with the low molecular weight heparin nadroparin.
Detailed Description
Severely ill patients admitted to the intensive care unit may develop an acute failure of kidney function. Renal function generally recovers if the acute illness improves. To bridge this period, renal function is temporarily replaced by continuous hemofiltration, so called continuous venovenous hemofiltration (CVVH). To remove toxic substances and fluids, the patient's blood flows through a circuit, containing a filter. Flow in the filter is regulated by the CVVH-device. Normally blood starts to clot as soon as it leaves the body. To prevent clotting of the blood in the filter, the blood has to be 'anticoagulated'. For this purpose, heparins are generally used. Heparins make the blood less likely to clot. Drawback of the use of heparins is that they not only prevent clotting of blood in the circuit and the filter, but also in the patient. Heparins thereby increase the risk of bleeding. Intensive care patients are at higher risk of bleeding due to a recent operation or trauma, ulcers in the mouth or the stomach, or abnormalities in their blood to the acute illness. Due to the continuous application of CVVH for days, anticoagulation is administered without interruption over prolonged periods of time. Studies report bleeding complications in 5 to 50% of the patients. As a result of bleeding, patients need blood transfusion and sometimes surgery. Control of bleeding is sometimes extremely difficult. An alternative to heparin is citrate, which allows regional anticoagulation of the circuit and the filter without an effect increasing the risk of bleeding for the patient. Anticoagulation with citrate is more complex, nurses need to follow a strict protocol.. Several small studies have shown that regional anticoagulation with citrate is associated with less bleeding and a longer filter survival. The use if citrate is however associated with a greater risk of metabolic complications, if the protocol is not strictly followed. Primary aim of the present study is to show in a larger group of intensive care patients whether the use of regional anticoagulation with citrate is safe compared to systemic anticoagulation with the low molecular weight heparin nadroparin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Acute
Keywords
kidney failure, acute, venovenous hemofiltration, hemorrhage, heparin, low-molecular-weight, nadroparin, citrates

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
215 (Actual)

8. Arms, Groups, and Interventions

Arm Title
citrate
Arm Type
Active Comparator
Arm Description
regional anticoagulation with citrate
Arm Title
nadroparin
Arm Type
Active Comparator
Arm Description
nadroparin is a low molecular weight heparin
Intervention Type
Drug
Intervention Name(s)
trisodium citrate
Other Intervention Name(s)
regional anticoagulation with citrate
Intervention Description
for regional anticoagulation of the extracorporeal CVVH circuit
Intervention Type
Drug
Intervention Name(s)
nadroparin
Other Intervention Name(s)
nadroparin is a low molecular weight heparin
Intervention Description
for anticoagulation of the extracorporeal CVVH circuit
Primary Outcome Measure Information:
Title
bleeding complications
Time Frame
during administration of study anticoagulant
Title
transfusion requirement
Time Frame
during administration of study anticoagulant
Title
filter survival
Time Frame
during hemofiltration
Secondary Outcome Measure Information:
Title
mortality
Time Frame
3-month and hospital admission

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Intensive care patients scheduled for continuous venovenous hemofiltration Exclusion Criteria: Severe pre-existent liver failure (cirrhosis Child C), acute liver dysfunction as occurring with septic shock is not a reason for exclusion Active bleeding or bleeding necessitating the infusion of two red blood cell units within 24 hours before starting hemofiltration or a fall in hemoglobin of > 0.5 mmol/l. A fall in hemoglobin/hematocrit as a result of fluid loading is not regarded as bleeding. Surgery within 24 h prior to CVVH. Patients needing full systemic anticoagulation (unfractionated heparin in a dose of > 10000 IU/day, or nadroparin > 3800 IU/day) for other reasons Expectation to die within 24 hours Chronic dialysis Proven or suspected heparin-induced thrombocytopenia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heleen M Oudemans-van Straaten, MD,PhD
Organizational Affiliation
Onze Lieve Vrouwe Gasthuis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Onze Lieve Vrouwe Gasthuis
City
Amsterdam
ZIP/Postal Code
1090HM
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
19114912
Citation
Oudemans-van Straaten HM, Bosman RJ, Koopmans M, van der Voort PH, Wester JP, van der Spoel JI, Dijksman LM, Zandstra DF. Citrate anticoagulation for continuous venovenous hemofiltration. Crit Care Med. 2009 Feb;37(2):545-52. doi: 10.1097/CCM.0b013e3181953c5e.
Results Reference
result
PubMed Identifier
33314078
Citation
Tsujimoto H, Tsujimoto Y, Nakata Y, Fujii T, Takahashi S, Akazawa M, Kataoka Y. Pharmacological interventions for preventing clotting of extracorporeal circuits during continuous renal replacement therapy. Cochrane Database Syst Rev. 2020 Dec 14;12(12):CD012467. doi: 10.1002/14651858.CD012467.pub3.
Results Reference
derived

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Safety and Efficacy of the Use of Regional Anticoagulation With Citrate in Continuous Venovenous Hemofiltration

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