- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01648036
Heparin Anticoagulation to Improve Outcomes in Septic Shock: The HALO Pilot
9. Juli 2014 aktualisiert von: 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.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Tatsächlich)
76
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Quebec, Kanada, G1J 1Z4
- Hôpital de l'Enfant-Jésus
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Manitoba
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Winnipeg, Manitoba, Kanada, R2H 2A6
- St. Boniface Hospital
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Winnipeg, Manitoba, Kanada, R3A 1R9
- Winnipeg Health Sciences Centre
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3H 3A7 and B3H 2Y9
- Capital Health - Queen Elizabeth II Health Sciences Centre
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Ontario
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Hamilton, Ontario, Kanada, L8L 2X2
- Hamilton General Hospital
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Hamilton, Ontario, Kanada, L8N 4A6
- St Joseph's Healthcare Hamilton
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Ottawa, Ontario, Kanada, K1H 8L6
- Ottawa Hospital General Campus
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Ottawa, Ontario, Kanada, K1Y 4E9
- Ottawa Hospital Civic Campus
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Toronto, Ontario, Kanada, M5B 1W8
- St Michael's Hospital
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre und älter (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- ≥ 18 years of age
- 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.
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:
- Consent declined
- Clinically apparent other forms of shock including cardiogenic, obstructive (massive pulmonary embolism, cardiac tamponnade, tension pneumothorax), hemorrhagic, neurogenic, or anaphylactic
- Received vasopressor therapy for greater than 36 hours prior to enrollment
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.
- Have an indication for therapeutic anticoagulation (e.g. ACS, acute VTE, mechanical valve, etc)
- Intent of the most responsible physician to prescribe rhAPC
- Have had a known or suspected adverse reaction to UFH including HIT
- Are currently enrolled in related trial
- Known or suspected cirrhosis, or chronic ascites
- 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.
- Terminal illness with a life expectancy of less than 3 months
- Are pregnant
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Verdreifachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Unfractionated Heparin
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Dose: 18 IU/kg/hr, continuous intravenous infusion.
Duration: up to 7 days or until ICU discharge or death
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Aktiver Komparator: Dalteparin
Standard of care
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Dose 5000 IU, subcutaneous, daily
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Feasibility of enrollment - to enrol an average of 2 patients per site per month over the duration of the study
Zeitfenster: 1 year
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The primary measure of feasibility is the ability of participating sites to enroll an average of 2 patients per month.
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1 year
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Feasibility(1) - Consent rate - will be considered adequate if 60% of eligible patients are enrolled in the HALO pilot
Zeitfenster: 1 year
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1 year
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Safety - Rate of major and minor bleeding events
Zeitfenster: Duration of ICU admission, or up to day +9
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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.
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Duration of ICU admission, or up to day +9
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Activation of coagulation - Thrombin-antithrombin (TAT) complexes
Zeitfenster: Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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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
Zeitfenster: Duration of study drug infusion or up to a maximum of 7 days
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Duration of study drug infusion or up to a maximum of 7 days
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Feasibility(3) - Time from randomization to initiation of study drug
Zeitfenster: the outcome will be assessed during the first 24 hours of enrollment
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The investigators will consider the time from randomization to study treatment initiation to be satisfactory if this interval is less than 4 hours.
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the outcome will be assessed during the first 24 hours of enrollment
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Activation of coagulation - Protein C concentration
Zeitfenster: Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Day 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Activation of Coagulation - Quantitative d-dimer
Zeitfenster: Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Markers of Inflammation (IL-6, IL-8, IL-10, and IL-17)
Zeitfenster: Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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Days 1, 2, 3, 5, 7, and 9 (or ICU discharge)
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ICU Mortality (Tertiary, descriptive outcome only)
Zeitfenster: Will be assessed at the time of ICU discharge or death; expected average length of ICU admission is 5.7 days
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Will be assessed at the time of ICU discharge or death; expected average length of ICU admission is 5.7 days
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Hospital Mortality (Tertiary, descriptive outcome only)
Zeitfenster: Will be assessed at the time of hospital discharge or death; expected average length of hospital admission is 14 days
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Will be assessed at the time of hospital discharge or death; expected average length of hospital admission is 14 days
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Change in MODS score (Tertiary, descriptive outcome only)
Zeitfenster: Will be assessed daily during admission to the ICU; expected average length of ICU admission is 5.7 days
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Will be assessed daily during admission to the ICU; expected average length of ICU admission is 5.7 days
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Hauptermittler: Ryan Zarychanski, MD MSc, University of Manitoba
- Hauptermittler: Dean Fergusson, PhD MHA, Ottawa Hospital Research Institute
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Juli 2012
Primärer Abschluss (Tatsächlich)
1. Januar 2014
Studienabschluss (Tatsächlich)
1. Februar 2014
Studienanmeldedaten
Zuerst eingereicht
14. Juli 2012
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
19. Juli 2012
Zuerst gepostet (Schätzen)
24. Juli 2012
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
10. Juli 2014
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
9. Juli 2014
Zuletzt verifiziert
1. Juli 2014
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Pathologische Prozesse
- Infektionen
- Systemisches Entzündungsreaktionssyndrom
- Entzündung
- Sepsis
- Schock, Septisch
- Schock
- Molekulare Mechanismen der pharmakologischen Wirkung
- Fibrinolytische Mittel
- Fibrinmodulierende Mittel
- Antikoagulanzien
- Heparin
- Calcium-Heparin
- Heparin, niedermolekular
- Tinzaparin
- Dalteparin
Andere Studien-ID-Nummern
- HCA2011/001
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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