Treatment for Blood Clots in the Veins of the Legs
Information source: National Institutes of Health Clinical Center (CC)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Embolism; Thrombophlebitis
Intervention: Recombinant Tissue Plasminogen Activator (Drug); Heparin (Drug); Warfarin (Drug)
Phase: Phase 1
Status: Completed
Sponsored by: National Institutes of Health Clinical Center (CC)
Summary
Acute deep venous thrombosis (ADVT) of the lower extremity is a common disorder. Traditional
treatment with anticoagulation therapy is effective in reducing the associated risk of
pulmonary embolism, but is ineffective in restoring patency of the venous system of the lower
extremity. While systemic thrombolytic therapy has been shown to be more effective than
anticoagulation, catheter directed local thrombolytic therapy is the most effective treatment
in restoring venous patency. Current treatment regimens are based on use of urokinase,
infused continuously through catheters imbedded into the thrombus. These treatment regimens
require doses on the order of 10,000,000 units of urokinase, resulting in significant
bleeding complications and prohibitive costs.
Experience at NIH with pulse-spray treatment of axillary subclavian venous thrombosis with
rtPA indicates that this is a highly effective and safe alternative thrombolytic regimen.
The proposed protocol is designed to evaluate the efficiency, safety, and doses of rtPA
associated with pulse spray directed rtPA treatment of the more extensive venous thrombosis
encountered in the lower extremity.
Clinical Details
Official title: Treatment of Acute Deep Vein Thrombosis of the Lower Extremity With Intraclot, Pulse-Sprayed Recombinant Tissue Plasminogen Activator, Plus Heparin and Warfarin: A Pilot Study
Study design: Treatment, Safety Study
Detailed description:
Acute deep venous thrombosis (ADVT) of the lower extremity is a common disorder. Traditional
treatment with anticoagulation therapy is effective in reducing the associated risk of
pulmonary embolism, but is ineffective in restoring patency of the venous system of the lower
extremity. While systemic thrombolytic therapy has been shown to be more effective than
anticoagulation, catheter directed local thrombolytic therapy is the most effective treatment
in restoring venous patency. Current treatment regimens are based on use of urokinase,
infused continuously through catheters imbedded into the thrombus. These treatment regimens
require doses on the order of 10,000,000 units of urokinase, resulting in significant
bleeding complications and prohibitive costs.
Experience at NIH with pulse-spray treatment of axillary subclavian venous thrombosis with
rtPA indicates that this is a highly effective and safe alternative thrombolytic regimen. The
proposed protocol is designed to evaluate the efficiency, safety, and doses of rtPA
associated with pulse spray directed rtPA treatment of the more extensive venous thrombosis
encountered in the lower extremity.
Eligibility
Minimum age: N/A.
Maximum age: N/A.
Gender(s): Both.
Criteria:
INCLUSION CRITERIA:
Patients must be 18 years or older. A negative pregnancy test is required for all female
patients of child-bearing age.
Only patients with first onset acute DVT will be accepted. Acute DVT-LE must be documented
by ultrasonography or venogram and will be defined as thrombosis of a major deep vein
segment above the popliteal vein less than 14 days since onset of symptoms or diagnosis.
Extension of thrombosis from the popliteal vein into calf veins is acceptable, but isolated
calf vein thrombosis will not be treated under this protocol, as the benefits of
thrombolytic therapy do not outweigh the risks.
EXCLUSION CRITERIA:
Current familial or acquired bleeding diathesis not attributable to heparin (prothrombin
time greater than 15 s, a PTT greater than 36 s, fibrinogen less than 150 mg/dL); platelet
count less than 50,000/gL unsupportable with platelet transfusions; creatinine greater than
2 mg/dL; severe hypertension (systolic greater than 200 mm Hg, or diastolic greater than
100 mm Hg); atrial fibrillation; known right-to-left shunts; pregnancy; breast feeding;
history of anaphylactic reactions to contrast media; history or evidence of heparin-induced
thrombocytopenia. Patients with underlying coagulopathy must be evaluated and cleared by
Dr. Horne or a consulting NIH hematologist before they can be accepted for the treatment
protocol.
Any of the following within the previous 2 weeks: gastrointestinal hemorrhage, active
peptic ulcer disease, hemoptysis, genitourinary tract hemorrhage (except microscopic
hematuria), major surgery, trauma, or biopsy of a non-compressible site.
Any of the following within the previous 2 months: cerebrovascular accident or hemorrhage.
Patients with hematocrits less than 30 percent or hemoglobin's less than 19 g/dl, based on
Clinical Center testing will not be asked to participate in the Thrombolytic Enzyme Kinetic
Study.
Locations and Contacts
National Institutes of Health Clinical Center (CC), Bethesda, Maryland 20892, United States
Additional Information
Related publications: Semba CP, Dake MD. Iliofemoral deep venous thrombosis: aggressive therapy with catheter-directed thrombolysis. Radiology. 1994 May;191(2):487-94. Chang R, Horne MK 3rd, Mayo DJ, Doppman JL. Pulse-spray treatment of subclavian and jugular venous thrombi with recombinant tissue plasminogen activator. J Vasc Interv Radiol. 1996 Nov-Dec;7(6):845-51. [No authors listed] Thrombolytic therapy in thrombosis: a National Institutes of Health consensus development conference. Ann Intern Med. 1980 Jul;93(1):141-4. No abstract available.
Starting date: February 1998
Ending date: January 2006
Last updated: March 3, 2008
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