跳至主要内容
临床试验/NCT00245856
NCT00245856已完成4 期

Treatment of Upper Extremity Deep-Vein Thrombosis

University of Oklahoma2 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2002年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
67
试验地点
2
主要终点
Percentage of Participants That Died at 3 Months

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with confirmed upper extremity DVT diagnosed by ultrasound imaging or venogram

排除标准

  • 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

研究组 & 干预措施

Treatment of Upper Extremity DVT

Experimental

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

干预措施: Dalteparin sodium injection (Drug)

Treatment of Upper Extremity DVT

Experimental

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

干预措施: Warfarin (Drug)

结局指标

主要结局

Percentage of Participants That Died at 3 Months

时间窗: 3 months

New Venous Thromboembolism at 3 Months

时间窗: 3 months

New DVT or PE at 3 months confirmed by diagnostic testing

次要结局

  • Bleeding Events(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Suman Rathbun

Professor of Medicine

University of Oklahoma

研究点 (2)

Loading locations...

相似试验

Treatment of Upper Extremity Deep-Vein Thrombosis | 临床试验