Septic Shock Clinical Trial
Official title:
Prospective Randomized Study to Assess Impact of Statins in Septic Shock
Sepsis is a common, expensive, frequently fatal and highly complex inflammatory syndrome
wherein multiple cellular and humoral pathways are involved. Since it's a multifactorial
syndrome merely blocking one of the various inflammatory pathways may not suffice to provide
effective treatment and this may partly explain why most of the adjunctive therapies
developed for severe sepsis have yielded disappointing results in rigorous clinical trials.
Statins have varied pleiotropic effects on the inflammatory mediators and there addition to
the current adjuvant therapies in septic shock may help in reduction of mortality. The
present trial aims to study survival benefit and changes in bio-marker levels in septic
shock.
Adult patients (>=18 years) in septic shock and admitted to ICU will be included in the
study. Patients will be randomized as per computer generated random number into the Drug
(Atorvastatin, 40 mg) or matched placebo group. Drug or placebo will be given to selected
patient via nasogastric tube for 7 days. Bio markers (Il-6, TNF-alpha) estimated during the
trial week (Days 1, 4, and 7). All clinical and study personnel and patients remained
blinded to the study group assignment throughout the trial.
Objectives:
- Study impact of statins on levels of biomarkers (IL-6 and TNF-α) of sepsis.
- Study survival benefit of statins in septic shock.
Introduction:
Sepsis is the leading cause of mortality in non-coronary ICUs. Mortality associated with
sepsis is still considerably high. Rising economic burden of managing sepsis is a major
concern. Statin is an anti-hyperlipidemic drug with pleiotropic effects. It has properties
like anti-inflammatory/oxidative, immunomodulatory effects, enhances endothelial function,
reduction in blood thrombogenicity, and increased nitric oxide (NO) bioavailability.
Available evidence suggests that statins may play a positive role in reduction of mortality
in sepsis. However, the multidimensional heterogeneous character of the available studies
does not allow drawing firm conclusions about its usefulness in sepsis and septic shock.
This randomized, double blinded, placebo controlled trial is an attempt to study the impact
of statins on mortality and biomarker levels in septic shock.
Details of material and methods:
Patients >= age 18 yrs meeting the American European consensus conference definition of
septic shock will be enrolled into the study. After the written informed consent from the
primary decision maker the patients will be randomized into either the drug or placebo
group. Each group will either receive Atorvastatin 40mg or a matched placebo for 7 days.
IL-6 and TNF alpha levels will be estimated on D1, D4 and D7 of the trial week. Relevant
clinical and laboratory (clinical biochemistry, hematological, coagulation parameters, LFT
and renal function tests) will be recorded simultaneously. Severity scores, event free days
(vasopressor, ventilation, dialysis, transfusion, parenteral nutrition), and mortality after
28 days of inclusion in study will be recorded.
Ethical Issues:
Written informed consent will be taken from either the patient (if possible) or from the
primary decision maker related to the patient.
Study population:
A total of 80 patients of septic shock admitted in ICU will be enrolled into this study.
Patients either admitted with septic shock or who develop septic shock during their stay in
ICU will be eligible for inclusion into the study. The statin and placebo group will have 40
patients each.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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