- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01073800
Using AtorVASTatin to Prevent VAscular Inflammatory OccLUSion in the Critically Ill (VASTVALUS)
Patients are admitted to the critical care unit of the hospital because of medical conditions that have a high likelihood of causing severe problems with blood flow, breathing, or brain function. These conditions also have a high likelihood of causing death. Approximately 10 to 15% of all critically ill patients die in hospital. A large amount of scientific evidence suggests that a substantial proportion of these deaths is due to a combination of blot clotting and inflammation in the blood vessels.
Statins are drugs that interfere with cholesterol and fat metabolism. Cholesterol and fat in the blood are associated with blood clotting and inflammation in the blood vessels. Statins are known to be very beneficial in improving the survival after heart attacks, and in preventing heart attacks.
The question that VASTVALUS asks is: do statins improve survival among all critically ill patients? In VASTVALUS, we will concentrate on patients that do not currently require a statin because of their medical condition e.g. after a heart attack, but we are concerned with the rest of the critically ill. In VASTVALUS, participating patients will receive either atorvastatin 80 mg daily or a placebo. Atorvastatin is a statin with a well-established record of safety and effectiveness. A placebo has no known medical activity. We will follow all patients in VASTVALUS to determine whether atorvastatin has any effect on the occurrence of death, stroke, heart attack, or kidney failure among the critically ill. Results from VASTVALUS will be shared with the medical community after the study is completed. As with all clinical trials, patients in VASTVALUS participate of their own choice, and can change their mind at any time.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Anticipé)
Phase
- Phase 2
- Phase 3
Contacts et emplacements
Lieux d'étude
-
-
Alberta
-
Edmonton, Alberta, Canada, T6G 2B7
- University of Alberta
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- 1. Men or women >18 years of age
2. Admitted to a critical care unit and requiring at least a 48 hour critical care unit stay for medical reasons. Medical reasons include:
- conditions of cardiovascular,
- respiratory, or
- neurologic impairment that require supportive care and observation.
Exclusion Criteria:
- 1. Hepatic failure (Childs-Pugh class C)
- 2. Rhabdomyolysis
- 3. Allergy or hypersensitivity to this drug or any of its components
- 4. Previous intolerance
- 5. Enrolment in another interventional trial
- 6. Contraindication to gastric and/or small bowel drug administration
- 7. MI as major diagnosis at admission (statin indicated)
- 8. Coronary artery intervention within previous 3 days
- 9. Currently receiving a statin or indicated (MI, dyslipidemia)
- 10. Pregnancy
- 11. personal or family history of hereditary muscular disorders
- 12. previous history of muscle toxicity with another HMG-CoA reductase Inhibitor
- 13. concomitant use of a fibrate or niacin
- 14. hypothyroidism
- 15. alcohol abuse
- 16. excessive physical exercise
- 17. renal impairment
- 18. diabetes with hepatic fatty change
- 19. surgery and trauma
- 20. frailty
- 21. situations where an increased plasma level of active ingredient may occur
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur placebo: placebo
|
placebo
|
|
Comparateur actif: atorvastatin 80 mg
active treatment
|
atorvastatin 80 mg per os daily
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
vascular occlusive events
Délai: 30 days
|
30 days
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
liver enzyme elevation
Délai: 30 days
|
30 days
|
|
rhabdomyolysis
Délai: 30 days
|
30 days
|
|
myalgias
Délai: 30 days
|
30 days
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Ischémie
- Processus pathologiques
- Nécrose
- Ischémie myocardique
- Maladies cardiaques
- Maladies cardiovasculaires
- Maladies vasculaires
- Maladies rénales
- Maladies urologiques
- Attributs de la maladie
- Infarctus du myocarde
- Infarctus
- Insuffisance rénale
- Maladie critique
- Mécanismes moléculaires de l'action pharmacologique
- Inhibiteurs d'enzymes
- Antimétabolites
- Agents anticholestérolémiants
- Agents hypolipidémiants
- Agents de régulation des lipides
- Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase
- Atorvastatine
Autres numéros d'identification d'étude
- VASTVALUS
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .