Overview
Use of Low Molecular Weight Heparin (Tinzaparin) to Treat Blood Clots in Patients With Kidney Failure
Status:
Terminated
Terminated
Trial end date:
2016-02-01
2016-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Blood clots in the leg veins, known as deep vein thrombosis, are important because they may travel to the lung (known as pulmonary embolism) and cause death. Blood clots are treated with blood thinners, or anticoagulants. The preferred treatment is an anticoagulant known as low molecular weight heparin (LMWH). LMWH is given by an injection under the skin, which is convenient for patients because they can self-administer this medication at home, and no blood testing is required. However, LMWH is cleared from the body through the kidneys, so patients who have kidney failure are generally not treated with LMWH because they may be at a higher risk of bleeding. One type of LMWH, known as tinzaparin, may be less dependent on the kidneys for clearance and may not increase in patients with kidney failure. The investigators would like to use tinzaparin to treat patients who have deep vein thrombosis or pulmonary embolism, and who also have kidney failure. The purpose of this study is to determine whether the blood thinning effects of tinzaparin build up, or accumulate, in patients with varying degrees of kidney failure compared to patients without kidney failure. The blood thinning effects will be measured using a blood test known as an anti-Xa level. Patients will be followed over the time they receive tinzaparin and those patients who are found to have potentially high levels of tinzaparin (based on the anti-Xa level) will have their tinzaparin dose adjusted. The investigators believe that the levels of tinzaparin will not accumulate to potentially dangerous levels in a significant number of patients with kidney failure.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
St. Joseph's Healthcare HamiltonCollaborators:
Heart and Stroke Foundation of Ontario
LEO PharmaTreatments:
Dalteparin
Heparin
Heparin, Low-Molecular-Weight
Tinzaparin
Criteria
Inclusion Criteria:- Adult patients 18 years of age or older
- Objectively confirmed VTE requiring anticoagulant therapy, including lower extremity
and upper extremity deep vein thrombosis (catheter and non-catheter related, including
dialysis access thrombosis [i.e., graft, fistula]); peripheral vein thrombosis (e.g.,
portal vein, mesenteric vein, cerebral vein thrombosis), and pulmonary embolism
Exclusion Criteria:
- Weight exceeding 105 kg
- Unstable declining renal function, defined as documented change in creatinine > 20% in
the past 3 months or clinical circumstances likely to be associated with change in
renal function, such as dehydration or severe intercurrent illness. Where no previous
creatinine values exist and the patient is otherwise stable, patients will not be
excluded on the basis of unknown previous renal function.
- Known allergy to heparin/LMWHs or history of heparin induced thrombocytopenia
- Treatment with UFH, LMWH, danaparoid, oral direct thrombin inhibitors for >48 h
- Bleeding requiring hospitalization or blood transfusion within 6 months(exception is
blood transfusion given in relation to surgical procedures within 6 months)
- History of intracerebral hemorrhage
- Known active liver disease (AST or ALT > 3 times the upper limit of normal, or
bilirubin > 50 umol/L)
- Known active peptic ulcer disease, with ongoing symptoms or need for anti-ulcer
medical therapy
- Thrombocytopenia (platelet count of < 100 x 109/L)
- Ongoing need for antiplatelet agents (clopidogrel, ticlopidine, aspirin > 325 mg
daily)
- Pregnancy or lactation
- Geographic inaccessibility
- Unable, or unwilling, to provide written informed consent