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Treatment of Upper Extremity Deep-Vein Thrombosis

Primary Purpose

Deep-Vein Thrombosis

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Dalteparin sodium injection
Warfarin
Sponsored by
University of Oklahoma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Deep-Vein Thrombosis focused on measuring Upper Extremity Deep-Vein Thrombosis, DVT, Fragmin, Deep-Vein Thrombosis, Thrombosis

Eligibility Criteria

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

Inclusion Criteria: Patients with confirmed upper extremity DVT diagnosed by ultrasound imaging or venogram Exclusion Criteria: Active, clinically significant bleeding Known hypersensitivity to heparin or low-molecular weight heparin Currently pregnant or less than 1 week post-partum Acquired bleeding diathesis Known inherited bleeding disorder Renal failure Extremes of weight Poor performance status Unable to return for repeat diagnostic testing or follow-up visits

Sites / Locations

  • Department of Veterans Affairs Medical Center
  • University of Oklahoma Health Science Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment of Upper Extremity DVT

Arm Description

Participants received dalterparin followed by warfarin or received dalterparin monotherapy for the treatment of upper extremity DVT

Outcomes

Primary Outcome Measures

Percentage of Participants That Died at 3 Months
New Venous Thromboembolism at 3 Months
New DVT or PE at 3 months confirmed by diagnostic testing

Secondary Outcome Measures

Bleeding Events
Total major bleeding rate

Full Information

First Posted
October 26, 2005
Last Updated
February 15, 2013
Sponsor
University of Oklahoma
Collaborators
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00245856
Brief Title
Treatment of Upper Extremity Deep-Vein Thrombosis
Official Title
Treatment of Upper Extremity Deep-Vein Thrombosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Oklahoma
Collaborators
Pfizer

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to document the long-term outcome or prognosis of patients diagnosed with upper extremity deep-vein thrombosis who are treated with Fragmin (dalteparin sodium injection) for three months.
Detailed Description
Upper extremity deep-vein thrombosis (DVT) is an increasingly common clinical problem and has been found to cause important pulmonary embolism in up to 36% of cases including fatal embolism. The major risk factor for development of DVT is presence of a central venous catheter in which up to 30% of patients may develop venous thrombosis. Peripherally inserted central catheters or (PICC) lines have been more frequently used in order to avoid the morbidity of central venous catheter insertion. There is little data on the incidence of DVT with these catheters, or effective treatment regimen. The purpose of this study is to document the long-term outcome or prognosis of patients diagnosed with upper extremity deep-vein thrombosis who are treated with Fragmin (dalteparin sodium injection) for three months. About 100 patients will be enrolled in this study at the University of Oklahoma. All patients with upper extremity DVT will be screened. Each will have a complete baseline and risk factor assessment. All patients will receive active study drug for a period of 3 months with reassessment of upper extremity DVT by ultrasound. All patients will participate for a period of 12 months with follow up visits at 5-7 day, and 1, 3, 6, 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep-Vein Thrombosis
Keywords
Upper Extremity Deep-Vein Thrombosis, DVT, Fragmin, Deep-Vein Thrombosis, Thrombosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
67 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment of Upper Extremity DVT
Arm Type
Experimental
Arm Description
Participants received dalterparin followed by warfarin or received dalterparin monotherapy for the treatment of upper extremity DVT
Intervention Type
Drug
Intervention Name(s)
Dalteparin sodium injection
Other Intervention Name(s)
Fragmin
Intervention Description
200units/kg subcutaneous daily for one month, followed by 150units/kg subcutaneous daily for two additional months or 200 units/kg subcutaneously daily for 5 days followed by warfarin.
Intervention Type
Drug
Intervention Name(s)
Warfarin
Intervention Description
Titrated to INR 2-3 through study month 3
Primary Outcome Measure Information:
Title
Percentage of Participants That Died at 3 Months
Time Frame
3 months
Title
New Venous Thromboembolism at 3 Months
Description
New DVT or PE at 3 months confirmed by diagnostic testing
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Bleeding Events
Description
Total major bleeding rate
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with confirmed upper extremity DVT diagnosed by ultrasound imaging or venogram Exclusion Criteria: Active, clinically significant bleeding Known hypersensitivity to heparin or low-molecular weight heparin Currently pregnant or less than 1 week post-partum Acquired bleeding diathesis Known inherited bleeding disorder Renal failure Extremes of weight Poor performance status Unable to return for repeat diagnostic testing or follow-up visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Suman W. Rathbun, M.D.
Organizational Affiliation
University of Oklahoma Health Science Center, Dept of Medicine/CardioVascular section
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Veterans Affairs Medical Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Facility Name
University of Oklahoma Health Science Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73117
Country
United States

12. IPD Sharing Statement

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Treatment of Upper Extremity Deep-Vein Thrombosis

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