- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01648036
Heparin Anticoagulation to Improve Outcomes in Septic Shock: The HALO Pilot
9 luglio 2014 aggiornato da: 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.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Effettivo)
76
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Quebec, Canada, G1J 1Z4
- Hôpital de l'Enfant-Jésus
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Manitoba
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Winnipeg, Manitoba, Canada, R2H 2A6
- St. Boniface Hospital
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Winnipeg, Manitoba, Canada, R3A 1R9
- Winnipeg Health Sciences Centre
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Nova Scotia
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Halifax, Nova Scotia, Canada, B3H 3A7 and B3H 2Y9
- Capital Health - Queen Elizabeth II Health Sciences Centre
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Ontario
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Hamilton, Ontario, Canada, L8L 2X2
- Hamilton General Hospital
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Hamilton, Ontario, Canada, L8N 4A6
- St Joseph's Healthcare Hamilton
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Ottawa, Ontario, Canada, K1H 8L6
- Ottawa Hospital General Campus
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Ottawa, Ontario, Canada, K1Y 4E9
- Ottawa Hospital Civic Campus
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Toronto, Ontario, Canada, M5B 1W8
- St Michael's Hospital
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
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
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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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Comparatore attivo: Dalteparin
Standard of care
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Dose 5000 IU, subcutaneous, daily
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Feasibility of enrollment - to enrol an average of 2 patients per site per month over the duration of the study
Lasso di tempo: 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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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Feasibility(1) - Consent rate - will be considered adequate if 60% of eligible patients are enrolled in the HALO pilot
Lasso di tempo: 1 year
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1 year
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Safety - Rate of major and minor bleeding events
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Ryan Zarychanski, MD MSc, University of Manitoba
- Investigatore principale: Dean Fergusson, PhD MHA, Ottawa Hospital Research Institute
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 luglio 2012
Completamento primario (Effettivo)
1 gennaio 2014
Completamento dello studio (Effettivo)
1 febbraio 2014
Date di iscrizione allo studio
Primo inviato
14 luglio 2012
Primo inviato che soddisfa i criteri di controllo qualità
19 luglio 2012
Primo Inserito (Stima)
24 luglio 2012
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
10 luglio 2014
Ultimo aggiornamento inviato che soddisfa i criteri QC
9 luglio 2014
Ultimo verificato
1 luglio 2014
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Processi patologici
- Infezioni
- Sindrome da risposta infiammatoria sistemica
- Infiammazione
- Sepsi
- Shock, settico
- Shock
- Meccanismi molecolari dell'azione farmacologica
- Agenti fibrinolitici
- Agenti modulanti la fibrina
- Anticoagulanti
- Eparina
- Eparina di calcio
- Eparina, a basso peso molecolare
- Tinzaparina
- Dalteparin
Altri numeri di identificazione dello studio
- HCA2011/001
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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