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

9 juli 2014 uppdaterad av: 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.

Studieöversikt

Status

Avslutad

Betingelser

Studietyp

Interventionell

Inskrivning (Faktisk)

76

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

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

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Trippel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Unfractionated Heparin
Dose: 18 IU/kg/hr, continuous intravenous infusion. Duration: up to 7 days or until ICU discharge or death
Aktiv komparator: Dalteparin
Standard of care
Dose 5000 IU, subcutaneous, daily
Andra namn:
  • Fragmin

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Feasibility of enrollment - to enrol an average of 2 patients per site per month over the duration of the study
Tidsram: 1 year
The primary measure of feasibility is the ability of participating sites to enroll an average of 2 patients per month.
1 year

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Feasibility(1) - Consent rate - will be considered adequate if 60% of eligible patients are enrolled in the HALO pilot
Tidsram: 1 year
1 year
Safety - Rate of major and minor bleeding events
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Ryan Zarychanski, MD MSc, University of Manitoba
  • Huvudutredare: Dean Fergusson, PhD MHA, Ottawa Hospital Research Institute

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 juli 2012

Primärt slutförande (Faktisk)

1 januari 2014

Avslutad studie (Faktisk)

1 februari 2014

Studieregistreringsdatum

Först inskickad

14 juli 2012

Först inskickad som uppfyllde QC-kriterierna

19 juli 2012

Första postat (Uppskatta)

24 juli 2012

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

10 juli 2014

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

9 juli 2014

Senast verifierad

1 juli 2014

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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