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临床试验/NCT01694459
NCT01694459Unknown4 期

Comparison of Low-dose Heparin Versus Standard Dose Heparin During Coronary Interventions (DEDICA Trial)

San Filippo Neri General Hospital1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
1,000
试验地点
1
主要终点
MACE + stent thrombosis + major bleeding (TIMI definition)

研究概览

简要总结

International guidelines support the use of a full-dose heparin (anticoagulants) during coronary intervention. However, a lower dose of heparin may be adequate, thanks to advances in angioplasty techniques and the widespread use of pretreatment with two antiplatelet agents.

Thus the investigators designed a study comparing safety and efficacy of standard dose heparin (100 UI/Kg) versus low-dose (50 UI/Kg) in patients undergoing coronary angioplasty who are on aspirin and clopidogrel at the time of the procedure.

详细描述

  • Patients undergoing coronary angioplasty will be randomised to standard vs. low-dose heparin. the study will include "all-comers" (patients with either stable angina or acute coronary syndromes); only patients with ST-elevation myocardial infarction will be excluded.
  • An ACT (activated clotting time) will be performed after the initial bolus of heparin: for the standard dose group the target ACT will be > 300 sec. (as recommended by guidelines) while for the low-dose the target ACT will be > 180 sec.

Aim of the study is to show equivalence in ischemic events between the two doses of heparin, in order to confirm the safety of lower dose of heparin in contemporary coronary interventions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

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

  • Stable angina, unstable angina or Non-ST elevation myocardial infarction undergoing coronary angioplasty.
  • Mandatory pretreatment with aspirin and clopidogrel

排除标准

  • ST elevation myocardial infarction
  • Coronary interventions with rotational atherectomy
  • Coronary interventions on chronic total occlusions (CTO)

研究组 & 干预措施

Standard dose heparin

Active Comparator

Bolus of 100 UI/Kg of heparin. Activated clotting time (ACT) > 300 sec. during the procedure

干预措施: Standard dose heparin (Drug)

Low-dose heparin

Experimental

Bolus of 50 UI/Kg heparin with a target ACT during the procedure of >200 sec.

干预措施: Low-dose heparin (Drug)

结局指标

主要结局

MACE + stent thrombosis + major bleeding (TIMI definition)

时间窗: 30 days

MACE (death, myocardial infarction, target vessel revascularization) + stent thrombosis + major bleeding (TIMI definition)

次要结局

  • MACE(30 days)
  • Major Bleeding(30 days)
  • Stent thrombosis(30 days)
  • CK-MB increase(30 days)

研究者

发起方
San Filippo Neri General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Vincenzo Pasceri

Attending Cardiologist

San Filippo Neri General Hospital

研究点 (1)

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