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Heparin Anticoagulation to Improve Outcomes in Septic Shock: The HALO Pilot

2014年7月9日 更新者:Dr. Ryan Zarychanski、University of Manitoba
Life-threatening infections account for 10% of all intensive care unit admissions and constitute the second more frequent cause of death in the ICU after heart diseases. The most common cause of death in patients admitted with life-threatening infections is multi-organ failure that is mediated by severe inflammation. Given the relationship between inflammation and blood clotting, blood-thinners (also called anticoagulants) have been used to decrease inflammation and the formation of small clots. Several lines of evidence suggest that heparin, a proven and inexpensive blood-thinner, may reduce improve survival in patients diagnosed with life-threatening infection. The primary objective of this study is to demonstrate the feasibility of enrolling patients in a large randomized controlled trial investigating heparin in patients with severe infections. In this study, patients with life-threatening infections will have an equal chance of receiving an intravenous infusion of heparin, or a low dose of a similar drug to prevent of blood clots while patients are immobile. The primary purpose of the study is to demonstrate that an average of 2 patients per site, per month, can be enrolled. Other measures of feasibility include the consent rate, the number of protocol violations that occur during the trial, and the number of dose reductions needed due to excessive anticoagulation. To study the biologic effects of heparin in patients with severe infection, specific laboratory markers will be measured and analyzed. If the feasibility of the trial is confirmed, a large randomized trial designed to tell if heparin can safely improve survival will be conducted. Given its low cost and availability, if heparin is shown to improve survival in patients with severe infection, adoption of this therapy on a global scale is anticipated.

研究概览

研究类型

介入性

注册 (实际的)

76

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Quebec、加拿大、G1J 1Z4
        • Hôpital de l'Enfant-Jésus
    • Manitoba
      • Winnipeg、Manitoba、加拿大、R2H 2A6
        • St. Boniface Hospital
      • Winnipeg、Manitoba、加拿大、R3A 1R9
        • Winnipeg Health Sciences Centre
    • Nova Scotia
      • Halifax、Nova Scotia、加拿大、B3H 3A7 and B3H 2Y9
        • Capital Health - Queen Elizabeth II Health Sciences Centre
    • Ontario
      • Hamilton、Ontario、加拿大、L8L 2X2
        • Hamilton General Hospital
      • Hamilton、Ontario、加拿大、L8N 4A6
        • St Joseph's Healthcare Hamilton
      • Ottawa、Ontario、加拿大、K1H 8L6
        • Ottawa Hospital General Campus
      • Ottawa、Ontario、加拿大、K1Y 4E9
        • Ottawa Hospital Civic Campus
      • Toronto、Ontario、加拿大、M5B 1W8
        • St Michael's Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. ≥ 18 years of age
  2. Refractory hypotension documented within 36 hours prior to enrolment that requires institution and ongoing use of vasopressor agents (phenylephrine, norepinephrine, vasopressin, epinephrine, or dopamine > 5 mcg/kg/min) at the time of enrolment. Refractory hypotension is defined as a systolic blood pressure < 90 mmHG or a systolic blood pressure more than 30 mmHg below baseline, or a mean arterial pressure less than 65 mmHG and receipt of greater than or equal to 2 litres of intravenous fluid for the treatment of hypotension.
  3. At least 1 other new organ dysfunction defined by the following:

    • Creatinine ≥ 150 µmol/L, or ≥ 1.5x the upper limit of normal or the known baseline creatinine, or < 0.5 ml/kg or urine output for 2 hours(Patients on chronic hemodialysis or peritoneal dialysis must meet one of the following criteria)
    • Need for invasive mechanical ventilation or a P/F ratio < 250
    • Platelets < 100 x109/L, or a drop of 50 x109/L in the 3 days prior to enrollment
    • Arterial pH < 7.30 or base deficit > 5 mmol/L in association with a lactate >/= to 3.0 mmol/L

Exclusion Criteria:

  1. Consent declined
  2. Clinically apparent other forms of shock including cardiogenic, obstructive (massive pulmonary embolism, cardiac tamponnade, tension pneumothorax), hemorrhagic, neurogenic, or anaphylactic
  3. Received vasopressor therapy for greater than 36 hours prior to enrollment
  4. Have a significant risk of bleeding as evidenced by one of the following:

    • Clinical: Surgery requiring general or spinal anesthesia within 24 hours prior to enrollment, or the potential need for such surgery in the next 24 hours; evidence of active bleeding; a history of severe head trauma requiring hospitalization; intracranial surgery, or stroke within 3 months before the study or any history of intracerebral arteriovenous malformation, cerebral aneurysm, or mass lesions of the central nervous system; a history of congenital bleeding diatheses; gastrointestinal bleeding within 6 weeks before the study unless corrective surgery had been performed; trauma considered to increase the risk of bleeding; presence of an epidural catheter
    • Laboratory: Platelet count < 30 x109/L, INR > 2.0, or baseline aPTT > 50 sec prior to enrollment.
  5. Have an indication for therapeutic anticoagulation (e.g. ACS, acute VTE, mechanical valve, etc)
  6. Intent of the most responsible physician to prescribe rhAPC
  7. Have had a known or suspected adverse reaction to UFH including HIT
  8. Are currently enrolled in related trial
  9. Known or suspected cirrhosis, or chronic ascites
  10. Use of any of the following medications or treatment regimens: unfractionated heparin to treat an active thrombotic event within 12 hours before the infusion enrollment; low-molecular-weight heparin at a higher dose than recommended for prophylactic use (as specified in the package insert) within 12 hours before the infusion; warfarin (if used within 7 days before study entry AND if the INR time exceeded the upper limit of the normal range for the institution); thrombolytic therapy within 3 days before the study, glycoprotein IIb/IIIa antagonists within 7 days before study entry; protein C or rhAPC within 24 hours before enrollment.
  11. Terminal illness with a life expectancy of less than 3 months
  12. Are pregnant

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Unfractionated Heparin
Dose: 18 IU/kg/hr, continuous intravenous infusion. Duration: up to 7 days or until ICU discharge or death
有源比较器:Dalteparin
Standard of care
Dose 5000 IU, subcutaneous, daily
其他名称:
  • 分片蛋白

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Feasibility of enrollment - to enrol an average of 2 patients per site per month over the duration of the study
大体时间:1 year
The primary measure of feasibility is the ability of participating sites to enroll an average of 2 patients per month.
1 year

次要结果测量

结果测量
措施说明
大体时间
Feasibility(1) - Consent rate - will be considered adequate if 60% of eligible patients are enrolled in the HALO pilot
大体时间:1 year
1 year
Safety - Rate of major and minor bleeding events
大体时间:Duration of ICU admission, or up to day +9
a.) Rates of major and minor bleeding will be adjudicated and will be considered in the context of monitored aPTTs: 1) in the context of aPTTs ≤95 seconds, the rate of major bleeding will be deemed acceptable if major bleeding occurs in ≤10% of patients; and 2) if >20% of patients require an initial (6 hour aPTT) dose reduction of the study drug due to an aPTT >95 seconds, this dose will be deemed infeasible as an initiation dose.
Duration of ICU admission, or up to day +9
Activation of coagulation - Thrombin-antithrombin (TAT) complexes
大体时间:Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Feasibility(2): Protocol Deviations - The investigators believe that an acceptable rate of protocol violations resulting in a non-scheduled dose reduction or interruption of the study drug to be less than 10% of all study drug dose adjustments
大体时间:Duration of study drug infusion or up to a maximum of 7 days
Duration of study drug infusion or up to a maximum of 7 days
Feasibility(3) - Time from randomization to initiation of study drug
大体时间:the outcome will be assessed during the first 24 hours of enrollment
The investigators will consider the time from randomization to study treatment initiation to be satisfactory if this interval is less than 4 hours.
the outcome will be assessed during the first 24 hours of enrollment
Activation of coagulation - Protein C concentration
大体时间:Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Activation of Coagulation - Quantitative d-dimer
大体时间:Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Markers of Inflammation (IL-6, IL-8, IL-10, and IL-17)
大体时间:Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
ICU Mortality (Tertiary, descriptive outcome only)
大体时间:Will be assessed at the time of ICU discharge or death; expected average length of ICU admission is 5.7 days
Will be assessed at the time of ICU discharge or death; expected average length of ICU admission is 5.7 days
Hospital Mortality (Tertiary, descriptive outcome only)
大体时间:Will be assessed at the time of hospital discharge or death; expected average length of hospital admission is 14 days
Will be assessed at the time of hospital discharge or death; expected average length of hospital admission is 14 days
Change in MODS score (Tertiary, descriptive outcome only)
大体时间:Will be assessed daily during admission to the ICU; expected average length of ICU admission is 5.7 days
Will be assessed daily during admission to the ICU; expected average length of ICU admission is 5.7 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Ryan Zarychanski, MD MSc、University of Manitoba
  • 首席研究员:Dean Fergusson, PhD MHA、Ottawa Hospital Research Institute

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2012年7月1日

初级完成 (实际的)

2014年1月1日

研究完成 (实际的)

2014年2月1日

研究注册日期

首次提交

2012年7月14日

首先提交符合 QC 标准的

2012年7月19日

首次发布 (估计)

2012年7月24日

研究记录更新

最后更新发布 (估计)

2014年7月10日

上次提交的符合 QC 标准的更新

2014年7月9日

最后验证

2014年7月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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