Fondaparinux 1,5 mg for the Prevention of Venous Thromboembolism (VTE) in Medical Patients With Renal Insufficiency
Primary Purpose
Medical Patients, Renal Insufficiency
Status
Terminated
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
fondaparinux
Sponsored by
About this trial
This is an interventional prevention trial for Medical Patients focused on measuring renal failure, medical patient, venous thromboembolism, prophylaxis, fondaparinux
Eligibility Criteria
Inclusion Criteria:
- Age > 60 years
- Acute medical disease requiring thromboprophylaxis according to international guidelines
- Anticipated immobilization of at least 4 days
- Renal insufficiency defined by creatinine clearance between 20 and 50 mL/min according the MDRD formula
- Written informed consent
Exclusion Criteria:
- Active bleeding or bleeding in the previous 3 months
- Known bleeding diathesis
- Platelet count < 100.000
- Ongoing treatment with unfractionated heparin, low molecular weight heparin, fondaparinux, or vitamin K antagonists
- Use of prophylactic doses of heparin, low molecular weight heparin, or fondaparinux in the previous 72 hours
- Life expectancy < 1 month
Sites / Locations
- University Of Insubria
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
fondaparinux
Arm Description
Outcomes
Primary Outcome Measures
major bleeding
Secondary Outcome Measures
symptomatic venous thromboembolism
Full Information
NCT ID
NCT00927602
First Posted
June 24, 2009
Last Updated
April 23, 2012
Sponsor
Università degli Studi dell'Insubria
1. Study Identification
Unique Protocol Identification Number
NCT00927602
Brief Title
Fondaparinux 1,5 mg for the Prevention of Venous Thromboembolism (VTE) in Medical Patients With Renal Insufficiency
Official Title
The Safety and Efficacy of Fondaparinux 1,5 mg for the Prevention of Venous Thromboembolism in Medical Patients With Renal Insufficiency
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Terminated
Why Stopped
study was stopped after enrolment of about 200 patients for slow recruitment
Study Start Date
April 2009 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
March 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Università degli Studi dell'Insubria
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Fondaparinux is a parenteral anticoagulant drug and is approved for the prevention of venous thromboembolism in high risk medical patients. A relevant proportion of medical patients have moderate to severe renal insufficiency, which is an independent risk factor for bleeding. This risk may be further increased when low molecular weight heparin or fondaparinux are administered in patients with severe renal insufficiency, defined by a creatinine clearance of lower than 30 mL/min. No clear indications are available to reduce such risk in patients who require thromboprophylaxis. A lower dose of fondaparinux, 1.5 mg daily, has been recently approved for the prevention of venous thromboembolism in the specific population of patients with a creatinine clearance between 20 and 50 mL/min (European Marketing Authorization). However, there are to our knowledge no clinical studies that have assessed the safety and efficacy of this reduced dosage in medical patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Medical Patients, Renal Insufficiency
Keywords
renal failure, medical patient, venous thromboembolism, prophylaxis, fondaparinux
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
206 (Actual)
8. Arms, Groups, and Interventions
Arm Title
fondaparinux
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
fondaparinux
Other Intervention Name(s)
Arixtra
Intervention Description
once daily sc injection, 1,5 mg, max 14 days
Primary Outcome Measure Information:
Title
major bleeding
Time Frame
up to 48 hours from last injection
Secondary Outcome Measure Information:
Title
symptomatic venous thromboembolism
Time Frame
last treatment dose
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 60 years
Acute medical disease requiring thromboprophylaxis according to international guidelines
Anticipated immobilization of at least 4 days
Renal insufficiency defined by creatinine clearance between 20 and 50 mL/min according the MDRD formula
Written informed consent
Exclusion Criteria:
Active bleeding or bleeding in the previous 3 months
Known bleeding diathesis
Platelet count < 100.000
Ongoing treatment with unfractionated heparin, low molecular weight heparin, fondaparinux, or vitamin K antagonists
Use of prophylactic doses of heparin, low molecular weight heparin, or fondaparinux in the previous 72 hours
Life expectancy < 1 month
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Walter Ageno, MD
Organizational Affiliation
Università degli Studi dell'Insubria
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Francesco Dentali, MD
Organizational Affiliation
Università degli Studi dell'Insubria
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alessandro Squizzato, MD
Organizational Affiliation
Università degli Studi dell'Insubria
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Of Insubria
City
Varese
ZIP/Postal Code
21100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
16439370
Citation
Cohen AT, Davidson BL, Gallus AS, Lassen MR, Prins MH, Tomkowski W, Turpie AG, Egberts JF, Lensing AW; ARTEMIS Investigators. Efficacy and safety of fondaparinux for the prevention of venous thromboembolism in older acute medical patients: randomised placebo controlled trial. BMJ. 2006 Feb 11;332(7537):325-9. doi: 10.1136/bmj.38733.466748.7C. Epub 2006 Jan 26.
Results Reference
background
PubMed Identifier
16670137
Citation
Lim W, Dentali F, Eikelboom JW, Crowther MA. Meta-analysis: low-molecular-weight heparin and bleeding in patients with severe renal insufficiency. Ann Intern Med. 2006 May 2;144(9):673-84. doi: 10.7326/0003-4819-144-9-200605020-00011.
Results Reference
background
PubMed Identifier
22925036
Citation
Ageno W, Riva N, Noris P, Di Nisio M, La Regina M, Arioli D, Ria L, Monzani V, Cuppini S, Lupia E, Giorgi Pierfranceschi M, Dentali F; FONDAIR study group. Safety and efficacy of low-dose fondaparinux (1.5 mg) for the prevention of venous thromboembolism in acutely ill medical patients with renal impairment: the FONDAIR study. J Thromb Haemost. 2012 Nov;10(11):2291-7. doi: 10.1111/j.1538-7836.2012.04908.x. Erratum In: J Thromb Haemost. 2016 Jan;14(1):225. Pierfranceschi, M G [corrected to Giorgi Pierfranceschi, M].
Results Reference
derived
Learn more about this trial
Fondaparinux 1,5 mg for the Prevention of Venous Thromboembolism (VTE) in Medical Patients With Renal Insufficiency
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