Landiolol in patients with septic shock resident in an intensive care unit (LANDI-SEP): study protocol for a randomized controlled trial
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu protokol klinické studie, časopisecké články
Grantová podpora
None
Amomed Pharma GmbH
PubMed
30454042
PubMed Central
PMC6245811
DOI
10.1186/s13063-018-3024-6
PII: 10.1186/s13063-018-3024-6
Knihovny.cz E-zdroje
- Klíčová slova
- Beta-blocker, Landiolol, Randomized controlled trial, Sepsis, Septic shock, Tachycardia,
- MeSH
- antiarytmika škodlivé účinky terapeutické užití MeSH
- beta blokátory škodlivé účinky terapeutické užití MeSH
- časové faktory MeSH
- jednotky intenzivní péče * MeSH
- klinické zkoušky, fáze IV jako téma MeSH
- krevní tlak účinky léků MeSH
- lidé MeSH
- močovina škodlivé účinky analogy a deriváty terapeutické užití MeSH
- morfoliny škodlivé účinky terapeutické užití MeSH
- multicentrické studie jako téma MeSH
- prospektivní studie MeSH
- randomizované kontrolované studie jako téma MeSH
- septický šok diagnóza farmakoterapie patofyziologie MeSH
- srdeční frekvence účinky léků MeSH
- vazokonstriktory terapeutické užití MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- protokol klinické studie MeSH
- Geografické názvy
- Evropa MeSH
- Názvy látek
- antiarytmika MeSH
- beta blokátory MeSH
- landiolol MeSH Prohlížeč
- močovina MeSH
- morfoliny MeSH
- vazokonstriktory MeSH
BACKGROUND: In patients with septic shock, the presence of an elevated heart rate (HR) after fluid resuscitation marks a subgroup of patients with a particularly poor prognosis. Several studies have shown that HR control in this population is safe and can potentially improve outcomes. However, all were conducted in a single-center setting. The aim of this multicenter study is to demonstrate that administration of the highly beta1-selective and ultrashort-acting beta blocker landiolol in patients with septic shock and persistent tachycardia (HR ≥ 95 beats per minute [bpm]) is effective in reducing and maintaining HR without increasing vasopressor requirements. METHODS: A phase IV, multicenter, prospective, randomized, open-label, controlled study is being conducted. The study will enroll a total of 200 patients with septic shock as defined by The Third International Consensus Definitions for Sepsis and Septic Shock criteria and tachycardia (HR ≥ 95 bpm) despite a hemodynamic optimization period of 24-36 h. Patients are randomized (1:1) to receive either standard treatment (according to the Surviving Sepsis Campaign Guidelines 2016) and continuous landiolol infusion to reach a target HR of 80-94 bpm or standard treatment alone. The primary endpoint is HR response (HR 80-94 bpm), the maintenance thereof, and the absence of increased vasopressor requirements during the first 24 h after initiating treatment. DISCUSSION: Despite recent studies, the role of beta blockers in the treatment of patients with septic shock remains unclear. This study will investigate whether HR control using landiolol is safe, feasible, and effective, and further enhance the understanding of beta blockade in patients with septic shock. TRIAL REGISTRATION: EU Clinical Trials Register; EudraCT, 2017-002138-22 . Registered on 8 August 2017.
Aixial s r o Brno Czech Republic
Amomed Pharma GmbH Vienna Austria
AOP Orphan Pharmaceuticals AG Wilhelminenstraße 91 2 f 1160 Vienna Austria
Department of Anesthesia and Intensive Care University Hospital of Modena Modena Italy
Department of Anesthesiology and Resuscitation 5 Azienda Ospedaliero Universitaria Pisana Pisa Italy
Department of Anesthesiology and Resuscitation 6 Azienda Ospedaliero Universitaria Pisana Pisa Italy
Department of Anesthesiology University Hospital Munich Munich Germany
Division of Transplant Anesthesia and Critical Care University School of Medicine Pisa Pisa Italy
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Heart rate control in septic shock-"every journey begins with a first step" (Confucius)