MedPath

Vitamin C, Thiamine, and Steroids in Sepsis

Phase 3
Completed
Conditions
Sepsis
Interventions
Registration Number
NCT03509350
Lead Sponsor
Emory University
Brief Summary

The VItamin C, Thiamine And Steroids in Sepsis (VICTAS) Study is a double-blind, placebo-controlled, adaptive randomized clinical trial designed to investigate the efficacy of the combined use of vitamin C, thiamine and corticosteroids versus indistinguishable placebos for patients with sepsis. The objective of this study is to demonstrate the efficacy of combination therapy using vitamin C, thiamine and corticosteroids in reducing mortality and improving organ function in critically ill patients with sepsis.

Detailed Description

Sepsis is an inflammatory syndrome with life threatening organ dysfunction resulting from a dysregulated host response to infection. The global burden is estimated to exceed 15 million cases annually. In the United States, the incidence is increasing and currently there are more 1,750,000 cases each year, with more than half requiring intensive care unit (ICU) admission. Further, sepsis cases account for 30%- 50% of all hospital deaths, making it the 3rd leading cause of death in the United States, and is the most expensive reason for hospitalization with annual expenditures exceeding $20 billion. Notably, even among those that do survive, many endure significant reductions in physical, emotional and cognitive quality of life. New therapeutic approaches to reduce the high morbidity and mortality of sepsis are needed.

Current management strategies focus on early aggressive fluid resuscitation, blood pressure support with vasopressors, early appropriate antibiotics, and the identification and control of infected sites. Though outcomes have improved with the bundled deployment of these strategies, mortality remains high at 20 - 30%. Despite over a hundred phase 2 and phase 3 clinical trials of pharmacological agents with the potential to improve sepsis outcomes, only antibiotics have demonstrated reproducible benefits.

The purpose of the current study is therefore to determine (or confirm) the efficacy of the combination therapy consisting of vitamin C, thiamine, and corticosteroids in the management of patients with circulatory and/or respiratory dysfunction resulting from sepsis. This subset of sepsis patients has been chosen because they are easily identified, have a high mortality, and consume significant critical care resources. As such, any improvements in outcomes attributed to effective therapies would be of great value to patients, as well as their care providers and healthcare systems. Further, because the promulgated therapies are composed of three inexpensive and readily available drugs, its efficacy would have important implications the management of sepsis in both well and poorly resourced settings worldwide.

The VItamin C, Thiamine And Steroids in Sepsis (VICTAS) Study is a double-blind, placebo-controlled, adaptive randomized clinical trial designed to investigate the efficacy of the combined use of vitamin C, thiamine and corticosteroids (the Treatment Protocol) versus indistinguishable placebos (the Control Protocol) for patients with sepsis. The trial will enroll up to 2000 participant and employs a novel endpoint that approximates a patient's risk of death based on the time spent on vasopressors or receiving respiratory support. Time spent on vasopressors or receiving respiratory support captures a patient's speed of recovery. Mortality rate is a key secondary endpoint for the trial.

Specific Aims

1. To demonstrate the efficacy of combination therapy using vitamin C, thiamine and corticosteroids to reduce the duration of cardiovascular and respiratory organ dysfunction in critically ill patients with sepsis.

2. To demonstrate the efficacy of combination therapy using vitamin C, thiamine and corticosteroids to reduce 30-day mortality in critically ill patients with sepsis.

Explicit subject consent for participation in long term telephone follow-up will be sought for all patients at all sites. Participation in long term outcome assessments is not required for participation in other aspects of the VICTAS study, i.e., patients may individually opt out of this portion of the study. In these participants a diverse array of neurocognitive outcomes will be assessed approximately 6 months after patient discharge. Evaluations will be done using a specially-designed battery of tests that evaluates key aspects of functioning and behavior and will be administered via phone by the Vanderbilt Long-Term Outcomes team, which will serve as the coordinating center for these follow-up assessments. The battery, which takes about 40 minutes to complete, will assess cognition, mental health, quality of life, and employment - all of which have been shown to be adversely affected in between one third and two thirds of survivors of sepsis.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
501
Inclusion Criteria
  • Suspected or confirmed infection as evidenced by ordering of blood cultures and administration of at least one antimicrobial agent

  • Anticipated or confirmed intensive care unit (ICU) admission

  • Acute respiratory or cardiovascular organ dysfunction attributed to sepsis as evidenced by at least one of the following requirements:

    1. Vasopressor Requirement - Continuous infusion of norepinephrine, epinephrine, vasopressin, dopamine, phenylephrine or other vasopressor agents at any dose for greater than 1 hour and required to maintain a mean arterial pressure ≥ 65 mm Hg despite intravenous crystalloid infusion of at least 1000cc
    2. Respiratory Support Requirement - Acute hypoxemic respiratory failure defined as persistent hypoxemia (partial pressure of arterial oxygen (PaO2)/fraction of inspired oxygen (FiO2) ≤ 300 or blood oxygen saturation (SpO2)/FiO2 ≤ 315) requiring (1) intubation and mechanical ventilation, or (2) positive pressure ventilation via tight-fitting face mask (i.e. continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) or (3) high flow nasal cannula ≥ 40 liter per minute (LPM) flow and FiO2 ≥ 0.40
Exclusion Criteria
  • Weight < 40 kilograms (kg)
  • Prior enrollment in this study
  • Qualifying organ dysfunction no longer present at the time subject would be randomized
  • Cardiovascular or respiratory organ failure caused by an illness other than sepsis
  • First episode of qualifying organ dysfunction during the current emergency department (ED) or ICU admission occurred > 24 hours before the subject could be randomized
  • Limitations of care (defined as refusal of cardiovascular and respiratory support modes) including "do not intubate" (DNI) status
  • Current hospitalization > 30 days at time of randomization
  • Chronic hypoxemia requiring supplemental non-invasive oxygen (nasal cannula or NIPPV) or home mechanical ventilation
  • Chronic cardiovascular failure requiring home mechanical hemodynamic support (e.g., LVAD) or home chemical hemodynamic support (e.g., milrinone)
  • Known allergy or contraindication to vitamin C, thiamine, and/or corticosteroids (including previously or currently diagnosed primary hyperoxaluria and/or oxalate nephropathy, or known/suspected ethylene glycol ingestion, or known glucose-6-phosphate dehydrogenase (G6PD) deficiency)
  • Use of vitamin C at a dose of > 1 gram daily within the 24 hours preceding first episode of qualifying organ dysfunction during a given ED or ICU admission
  • Chronic disease/illness that, in the opinion of the site investigator, have an expected lifespan of < 30 days unrelated to current sepsis diagnosis (e.g., stage IV malignancy, neurodegenerative disease, etc.)
  • Pregnancy or known active breastfeeding
  • Prisoner or Incarceration
  • Current participation in another interventional research study
  • Inability or unwillingness of subject or legal surrogate/representative to give written informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control ProtocolThiamine PlaceboA placebo to match the VICTAS intervention will be administered for four days or until ICU discharge. During the treatment period, if an indication for steroids exist, the treating physicians are permitted to initiate open-label corticosteroid therapy based on local practice and international guidelines. If this occurs, the hydrocortisone/placebo will be withheld and subjects will be started on open-label corticosteroids.
Control ProtocolHydrocortisone PlaceboA placebo to match the VICTAS intervention will be administered for four days or until ICU discharge. During the treatment period, if an indication for steroids exist, the treating physicians are permitted to initiate open-label corticosteroid therapy based on local practice and international guidelines. If this occurs, the hydrocortisone/placebo will be withheld and subjects will be started on open-label corticosteroids.
Control ProtocolVitamin C PlaceboA placebo to match the VICTAS intervention will be administered for four days or until ICU discharge. During the treatment period, if an indication for steroids exist, the treating physicians are permitted to initiate open-label corticosteroid therapy based on local practice and international guidelines. If this occurs, the hydrocortisone/placebo will be withheld and subjects will be started on open-label corticosteroids.
Treatment ProtocolVitamin CParticipants randomized to the treatment protocol will receive the VICTAS Intervention, consisting of intravenous vitamin C, thiamine, and hydrocortisone for four days or until ICU discharge.
Treatment ProtocolThiamineParticipants randomized to the treatment protocol will receive the VICTAS Intervention, consisting of intravenous vitamin C, thiamine, and hydrocortisone for four days or until ICU discharge.
Treatment ProtocolHydrocortisoneParticipants randomized to the treatment protocol will receive the VICTAS Intervention, consisting of intravenous vitamin C, thiamine, and hydrocortisone for four days or until ICU discharge.
Primary Outcome Measures
NameTimeMethod
Vasopressor and Ventilator-free Days (VVFD)Up to Day 30

The primary outcome measure is VVFD in the first 30 days after the start of treatment. The endpoint was recorded to the nearest day. Participants who died are scored zero days, even if there was a period during which the participant was alive and free of vasopressors and mechanical ventilation. Participants who must return to ventilation and/or vasopressors had their counters reset at zero days.

Secondary Outcome Measures
NameTimeMethod
Mortality at 30 DaysDay 30

The number of participants who did not survive until Day 30 is compared between study arms.

Intensive Care Unit (ICU) MortalityDay 30

The number of participants who died while in the ICU is compared between study arms.

Length of ICU StayDay 30

The number of days that participants were in the ICU is compared between study arms.

Controlled Oral Word Association Test (COWAT) ScoreDay 180

Language is assessed with the Controlled Oral Word Association Test (COWAT). Participants generate words beginning with selected letters within 60 seconds. Generating a higher number of words indicates greater language skills.

Mortality at 180 DaysDay 180

The number of participants who did not survive until Day 180 is compared between study arms.

Digit Span Test ScoreDay 180

The Digit Span Test is used to assesses attention. In the Digit Span Test, participants are read a series of numbers and are asked to repeat them back in the same order. The Digit Span test is scored by the number of digits the participant is able to remember in each test. Higher scores indicate greater ability to pay attention and to remember sequences. The average adult can remember about 7 numbers, plus or minus two, without making an error.

Number of Participants With Delirium Assessed With the DeliriumTelephone Confusion Assessment Method (CAM)Day 180

The Telephone CAM evaluates dementia with 9-items, where additional questions are asked if symptoms are present. Rather than providing a summary score, if participants exhibit signs of a change in mental status which fluctuates and they experience inattention, along with disorganized thinking or altered level of consciousness, delirium is suggested.

Hayling Test ScoreDay 180

Executive function is assessed with the Hayling Test. The Hayling Test includes two parts of 15 items each where participants complete sentences by providing the missing word. The test is scored as the amount of time it takes, in seconds, to recite a correct response and the appropriateness of the response (in Part 2). Scaled scores range from 1 to 10 where 1 = impaired, 6 = average, and 10 = very superior.

Wechsler Memory Scale III - Delayed Recall Logical Memory ScoreDay 180

Memory is assessed with the Logical Memory subtest from the Wechsler Memory Scale III. Participants listened to two short paragraphs and were asked to recall details from each story after 30 minutes. Scores represent the number of correctly remembered details. Total scores range from 0 to 25 with higher scores reflecting better memory.

Katz Index of Independence in Activities of Daily Living (ADL) ScoreDay 180

Activities of daily living is assessed with the Katz ADL instrument. The Katz ADL has 6 items asking if participants can perform daily tasks independently. Responses are scored as 1 = yes and 0 = no. Total scores range from 0 to 6 with higher scores indicating greater independence.

Functional Activities Questionnaire (FAQ) ScoreDay 180

Instrumental activities of daily living is assessed with the Functional Activities Questionnaire (FAQ). The FAQ includes 10 items which are scored on a scale from 0 to 3 where 0 = normal and 3 = dependent. Total scores range from 0 to 30 and lower scores indicate that the respondent is able to perform daily activities. A score of 9 (where the person is dependent in 3 activities) is used as a cut-point indicating impairments with functioning.

Posttraumatic Stress Disorder-8 (PTSD-8) ScoreDay 180

Posttraumatic Stress Disorder (PTSD) is assessed with the Posttraumatic Stress Disorder - 8 instrument. The PTSD-8 includes 8 items which are answered on a 4 point scale where 01 = not at all and 3 = all of the time. Total scores range from 0 to 24 where higher scores indicate greater symptoms of PTSD.

Length of Hospital StayDay 30

The number of days that participants were in the hospital is compared between study arms.

Number of Participants EmployedDay 180

The Employment Questionnaire is a brief measure of the participant's employment history and ability or capacity to work. The number of participants who indicated being employed are presented here.

Patient-Reported Outcomes Measurement Information System (PROMIS) Depression 6Day 180

Depression is assessed with the PROMIS Depression 6 instrument. This tool includes 6 items with response options on a scale of 1 to 5. Total raw scores range from 6 to 30 with higher scores indicating greater symptoms of depression.

Telephone Interview for Cognitive Status (TICS)Day 180

The Telephone Interview for Cognitive Status (TICS) is an 11-item instrument assessing orientation. Correct responses to the items are scored in a variety of ways, depending on how much of the response is correct. Total scores range from 0 to 41 with higher scores indicating increased cognitive orientation.

Wechsler Adult Intelligence Scale (WAIS)-IV Similarities ScoreDay 180

Reasoning is assessed with the WAIS-IV Similarities instrument. Participants were asked to explain how two words are alike. Responses are scored according to how correct they are, with a score of 0 for incorrect answers. After 3 consecutive scores of 0 the survey is stopped. Total raw scores vary depending on the number of word pairs presented. Higher scores indicate better performance. Scores will be compared between study arms.

EuroQol, 5 Dimension (EQ-5D) Visual Analog Scale ScoreDay 180

Quality of life is assessed with the Visual Analog Scale of the EuroQol, 5 dimension (EQ-5D) questionnaire. The EQ-5D asks about 5 dimensions of health (mobility, self-care, usual activities, pain, and depression). The questionnaire includes a visual analog scale where respondents rate their current health where 0 = worst health imaginable and 100 = best health imaginable.

Trial Locations

Locations (43)

University of Arizona

🇺🇸

Tucson, Arizona, United States

Yale New Haven Hospital

🇺🇸

New Haven, Connecticut, United States

Christiana Care

🇺🇸

Newark, Delaware, United States

Oregon Health Sciences University

🇺🇸

Portland, Oregon, United States

Lousiana State University

🇺🇸

New Orleans, Louisiana, United States

University of Utah

🇺🇸

Salt Lake City, Utah, United States

Virginia Commonwealth University

🇺🇸

Richmond, Virginia, United States

Baystate Health

🇺🇸

Springfield, Massachusetts, United States

Vanderbilt University Medical Center

🇺🇸

Nashville, Tennessee, United States

Montefiore Medical Center Weiler

🇺🇸

Bronx, New York, United States

Montefiore Medical Center Moses

🇺🇸

Bronx, New York, United States

Medstar Washington Hospital Center

🇺🇸

Washington, District of Columbia, United States

Maricopa Integrated Health System

🇺🇸

Phoenix, Arizona, United States

Stanford University

🇺🇸

Stanford, California, United States

Bon Secours

🇺🇸

Richmond, Virginia, United States

Wake Forest University

🇺🇸

Winston-Salem, North Carolina, United States

Sentara Healthcare

🇺🇸

Norfolk, Virginia, United States

University of Florida Jacksonville

🇺🇸

Jacksonville, Florida, United States

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

David Geffen School of Medicine at UCLA

🇺🇸

Los Angeles, California, United States

Emory Saint Joseph's Hospital

🇺🇸

Atlanta, Georgia, United States

Piedmont Healthcare

🇺🇸

Atlanta, Georgia, United States

Johns Hopkins Hospital

🇺🇸

Baltimore, Maryland, United States

Grady Memorial Hospital

🇺🇸

Atlanta, Georgia, United States

Emory University Hospital

🇺🇸

Atlanta, Georgia, United States

Ohio State University Wexner Medical Center

🇺🇸

Columbus, Ohio, United States

University of Pennsylvania Health System Hospital

🇺🇸

Philadelphia, Pennsylvania, United States

Temple University

🇺🇸

Philadelphia, Pennsylvania, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Cleveland Clinic

🇺🇸

Cleveland, Ohio, United States

Duke University

🇺🇸

Durham, North Carolina, United States

Hennepin County Medical Center

🇺🇸

Minneapolis, Minnesota, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

University of Colorado Denver

🇺🇸

Denver, Colorado, United States

Denver Health

🇺🇸

Denver, Colorado, United States

University of Maryland School of Medicine

🇺🇸

Baltimore, Maryland, United States

Johns Hopkins Bayview

🇺🇸

Baltimore, Maryland, United States

Henry Ford Health System

🇺🇸

Detroit, Michigan, United States

University of Cincinnati Physicians Company

🇺🇸

Cincinnati, Ohio, United States

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

University of Nebraska Medical Center

🇺🇸

Omaha, Nebraska, United States

Intermountain Medical Center

🇺🇸

Murray, Utah, United States

Thomas Jefferson University

🇺🇸

Philadelphia, Pennsylvania, United States

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