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

9 lipca 2014 zaktualizowane przez: 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.

Przegląd badań

Status

Zakończony

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

76

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • 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

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

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

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Potroić

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Unfractionated Heparin
Dose: 18 IU/kg/hr, continuous intravenous infusion. Duration: up to 7 days or until ICU discharge or death
Aktywny komparator: Dalteparin
Standard of care
Dose 5000 IU, subcutaneous, daily
Inne nazwy:
  • Fragmin

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Feasibility of enrollment - to enrol an average of 2 patients per site per month over the duration of the study
Ramy czasowe: 1 year
The primary measure of feasibility is the ability of participating sites to enroll an average of 2 patients per month.
1 year

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Feasibility(1) - Consent rate - will be considered adequate if 60% of eligible patients are enrolled in the HALO pilot
Ramy czasowe: 1 year
1 year
Safety - Rate of major and minor bleeding events
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

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

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 lipca 2012

Zakończenie podstawowe (Rzeczywisty)

1 stycznia 2014

Ukończenie studiów (Rzeczywisty)

1 lutego 2014

Daty rejestracji na studia

Pierwszy przesłany

14 lipca 2012

Pierwszy przesłany, który spełnia kryteria kontroli jakości

19 lipca 2012

Pierwszy wysłany (Oszacować)

24 lipca 2012

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

10 lipca 2014

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

9 lipca 2014

Ostatnia weryfikacja

1 lipca 2014

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Unfractionated heparin

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