A Phase 2 interventional study of Azithromycin on admission - not enrolled in the RCT in Systemic Inflammatory Response Syndrome, sponsored by VA Office of Research and Development. Terminated at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-04-21.
Sponsored by VA Office of Research and Development · Phase 2, Interventional, and Treatment
The purpose of this study is to determine whether macrolide treatment of patients with severe sepsis has an advantageous immunomodulatory and clinical effect compared to severe septic patients without macrolide therapy. Our main hypothesis is macrolide use in addition to standard therapy in severe septic patients has an advantageous immunomodulatory and clinical effect compared to patients with severe sepsis not treated with a macrolide.
In recent studies, the significant effects of macrolide antibiotics (azithromycin) on immune response, unrelated to their anti-microbial properties, have been appreciated. Clinical trials of macrolides added to -lactams in bacteremic Streptococcus pneumoniae community-acquired pneumonia (CAP) have consistently demonstrated an absolute risk reduction in mortality of 15% in most populations. Several cytokines including tumor necrosis factor (TNF) interleukin (IL) -1 and IL-8 which are generally proinflammatory and IL-6 and IL-10, which tend to be anti-inflammatory have been associated with sepsis. TNF is a cytokine that for a number of reasons is thought to play a central role in the pathogenesis of sepsis and septic shock. TNF concentrations are increased during clinical and experimental sepsis and increasing concentrations and especially persistence of high concentrations of TNF during sepsis are associated with decreased survival. Therefore, our primary aim is to determine whether macrolide treatment of patients with severe sepsis has an advantageous immunomodulatory and clinical effect compared to severe septic patients without macrolide therapy. Our main hypothesis is macrolide use in addition to standard therapy in severe septic patients has an advantageous immunomodulatory and clinical effect compared to patients with severe sepsis not treated with a macrolide.
1,899 studies on the registry are indexed under Sepsis; 462 are open to participants now.
This study's planned enrollment of 100 is close to the median of 105 across 896 interventional studies indexed under Sepsis.
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Of its 206 completed or terminated interventional studies of FDA-regulated products, 180 (87%) have results posted.
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SIRS is defined as two or more of:
Presence of one or more sepsis-associated organ failure. The onset of the first sepsis-associated organ failure must occur within the 48-hour period immediately preceding initiation of study drug infusion. A patient must have an organ failure attributable to the sepsis episode. The organ failure must be newly developed and not explained by underlying disease processes or by effects of concomitant therapy.
Adequate fluid resuscitation or adequate intravascular volume is defined as either pulmonary arterial wedge pressure 12 mm Hg or central venous pressure 8 mm Hg. Vasopressors is defined as dopamine 5 g/kg/min or any dose of norepinephrine, epinephrine, or phenylephrine. Dobutamine is not considered a vasopressor.
Exclusion Criteria:
Immunosuppression as defined by:
Standard antibiotic therapy +Azithromycin 500 mg intravenously daily for 5 days
Other: Azithromycin on admission - not enrolled in the RCT
Standard antibiotic therapy
One dose of azithromycin prior to inclusion to the RCT
Also known as: Arm 3
Change in cytokines expression
Time frame: Between admission and day five of treatment
28-day mortality
Time frame: 28 days or discharge
This study is terminated, as verified in Apr 2017. You cannot join it, but the record below documents what was studied.
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VA Office of Research and Development