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临床试验/NCT07388056
NCT07388056已完成不适用

Efficacy and Safety of Extended Anticoagulant Therapy in Cancer Associated Thrombosis-A Ten Year Retrospective Study.

Thammasat University0 个研究点目标入组 169 人开始时间: 2012年1月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
169
主要终点
Recurrent thrombosis

研究概览

简要总结

The goal of this observational study is to learn about the long-term efficacy and safety of extended anticoagulant treatment in patients with cancer associated thrombosis. (CAT) The main question it aims to answer is:

• Does extended prophylactic dose anticoagulant provide comparable efficacy and safety to therapeutic dosing after 6-month treatment of anticoagulant? The medical record data of participants who's already received for at least 6-month anticoagulant treatment upon regular medical care for CAT will be collected and analyzed about their recurrent thrombosis, anticoagulant related bleeding, and survival outcome.

详细描述

Adult patients aged ≥18 years with histopathological confirmed cancer, treated at Thammasat University Hospital and Panyananthaphikkhu Chonprathan Medical Center between January 2012 and December 2022, were eligible for inclusion.

Patients were initially screened using ICD-10 diagnostic codes C00-D009 for malignancy in conjunction with codes for venous thromboembolism (I82.-, other venous embolism and thrombosis; K55.0, mesenteric vein thrombosis; I82.0, hepatic vein thrombosis; K75.1, phlebitis of the portal vein; and I26.-, pulmonary embolism). Eligible patients required to have a radiologically confirmed diagnosis of cancer-associated thrombosis (CAT) and to have received anticoagulation therapy for at least six months. Clinical data were extracted from the Computerized Provider Order Entry (CPOE) system.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

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

  • Here's a polished version of your Inclusion and

排除标准

  • section with grammar, spelling, and phrasing corrected for clarity and formal research style:
  • Inclusion Criteria
  • Adult patients aged ≥18 years
  • Histopathologically confirmed cancer
  • Radiologically confirmed diagnosis of cancer-associated thrombosis (CAT)
  • Received anticoagulation therapy for at least six months Exclusion Criteria
  • Patients who do not meet the inclusion criteria

研究组 & 干预措施

Therapeutic dose anticoagulant group

including patients with the standard therapeutic dose-administered after the initial six-month treatment period.

干预措施: Anticoagulant (Drug)

Prophylactic dose anticoagulant group

including patients with the doses lower than therapeutic dose-administered at any point after the initial six-month treatment period.

干预措施: Anticoagulant (Drug)

结局指标

主要结局

Recurrent thrombosis

时间窗: After completing 6-month of treatment to the time that anticoagulant stop or recurrent thrombosis occurred through study completion, at the end of December 2025.

cumulative incidence of recurrent thrombosis

次要结局

  • Anticoagulant related bleeding(After completing 6-month of treatment to the time that anticoagulant stop or bleeding occurred through study completion, at the end of December 2025.)
  • Overall survival(The time from VTE diagnosis to last follow up or die through study completion, at the end of December 2025.)

研究者

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

Lantarima Bhoopat

Hematology, Internal medicine, Faculty of medicine

Thammasat University

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