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临床试验/NCT00625248
NCT00625248已完成不适用

A Prospective Evaluation of Bleeding Risk of Anticoagulant and Antiplatelet Therapy for Interventional Techniques

Pain Management Center of Paducah1 个研究点 分布在 1 个国家目标入组 12,000 人开始时间: 2008年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
12,000
试验地点
1
主要终点
To evaluate for differences between the patients undergoing interventional techniques with or without anticoagulant or antiplatelet therapy.

研究概览

简要总结

This study will evaluate bleeding risk and differences in outcomes in patients receiving and not receiving anticoagulant or antiplatelet therapy

详细描述

  1. To evaluate bleeding risk in interventional procedures in patients with or without antiplatelet and/or anticoagulant therapy.
  2. To evaluate differences in outcomes in patients not receiving any anticoagulant or antiplatelet therapy compared to patients receiving various types of drugs with anticoagulant or antiplatelet therapeutic effects.
  3. To evaluate and compare the adverse event profiling all patients.

研究设计

研究类型
Observational
时间视角
Prospective

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

  • Subjects undergoing interventional techniques. Subjects who were able to give voluntary, written informed consent.

排除标准

  • All those things, patients on heparin, dextran, and low molecular heparin

研究组 & 干预措施

no anthithrombotic

procedures where there were no antithrombotics

干预措施: Antithrombotics (Drug)

Antithrombotic - continued

patients who are on antithrombotics

干预措施: Antithrombotics (Drug)

Discontinued Antithrombotic

Patients who were on antithrombotics but have been discontinued

干预措施: Antithrombotics (Drug)

结局指标

主要结局

To evaluate for differences between the patients undergoing interventional techniques with or without anticoagulant or antiplatelet therapy.

时间窗: 24 months

次要结局

  • To assess adverse events in all patients.(24 months)

研究者

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

Laxmaiah Manchikanti, MD

Medical Director

Pain Management Center of Paducah

研究点 (1)

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