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Ascorbic Acid, Corticosteroids, and Thiamine in Sepsis (ACTS) Trial

Primary Purpose

Sepsis, Septic Shock, Metabolic Disturbance

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
vitamin C, vitamin B1, hydrocortisone
Normal saline
Sponsored by
Beth Israel Deaconess Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring Sepsis, Metabolic Resuscitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adult patient (age ≥ 18 years)
  2. Suspected (cultures drawn and antibiotic given) or confirmed (via culture results) infection
  3. Receiving vasopressor (norepinephrine, phenylephrine, epinephrine, dopamine, angiotensin II or vasopressin)

Exclusion Criteria:

  1. Member of a protected population (pregnant, prisoner)
  2. Known kidney stones within the past 1 year (except for asymptomatic, incidentally noted stones on imaging)
  3. End stage renal disease (ESRD) requiring dialysis
  4. Known Glucose-6-Phosphate Dehydrogenase deficiency
  5. Known Hemachromatosis
  6. Comfort Measures Only status
  7. Anticipated death within 24-hours despite maximal therapy (as determined by the enrolling physician)
  8. Receiving supplemental thiamine in a dose greater than that contained in a multivitamin
  9. Clinical indication for steroids (e.g. chronic use) as determined by the clinical team providing this drug
  10. Clinical indication for thiamine as determined by the clinical team providing this drug
  11. Clinical indication for ascorbic acid as determined by the clinical team providing this drug
  12. Known allergy to vitamin C, hydrocortisone, or thiamine

Sites / Locations

  • Mayo Clinic - Arizona
  • Brigham and Women's Hospital
  • Beth Israel Deaconess Medical Center
  • Mount Auburn Hospital
  • Detroit Receiving Hospital
  • Harper University Hospital
  • Henry Ford Hospital
  • Sinai Grace Hospital
  • Beaumont Hospital
  • North Shore University Hospital
  • Long Island Jewish Hospital
  • University Of Pittsburgh Medical Center
  • The University of Texas Health Science Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vitamin C, Vitamin B1, Corticosteroids

Placebo

Arm Description

The combination of vitamin C, vitamin B1, hydrocortisone : Vitamin C (ascorbic acid) 1.5g every 6 hours x 4-days Vitamin B1 (thiamine) 100mg every 6 hours x 4-days Hydrocortisone 50mg every 6 hours x 4-days

Normal Saline Solution (0.9%NaCl) in a volume to match all experimental arm components

Outcomes

Primary Outcome Measures

Sequential Organ Failure Assessment (SOFA) Score at Baseline and 72 Hours
Sequential Organ Failure Assessment (SOFA) Score at Baseline and 72 Hours. The SOFA score ranges from a minimum of 0 to a maximum of 24, with higher scores meaning worse outcomes.

Secondary Outcome Measures

Renal Failure
Development of renal failure as defined by a Kidney Disease Improving Global Outcomes [KDIGO] stage 3 or higher. There are 3 stages in the KDIGO scale with stage 3 being the worst (corresponds to renal failure). Stage 1- serum creatinine 1.5 to 1.9 times baseline OR an increase in serum creatinine ≥ 0.3 mg/dL OR urine output < 0.5ml/kg/hour for 6-12 hours. Stage 2- serum creatinine 2.0-2.9 times baseline OR urine output <0.5mg/kg/hour for ≥ 12 hours Stage 3- serum creatinine 3.0 times baseline (or serum creatinine of more than or equal to 4.0 mg/dl with an acute increase of at least 0.5 mg/dl) (OR) Urine output less than 0.3 ml/kg/hour for 24 hours or anuria for 12 hours or new renal replacement therapy
30-day Mortality
Mortality rate

Full Information

First Posted
December 27, 2017
Last Updated
January 29, 2021
Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Open Philanthropy
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1. Study Identification

Unique Protocol Identification Number
NCT03389555
Brief Title
Ascorbic Acid, Corticosteroids, and Thiamine in Sepsis (ACTS) Trial
Official Title
Ascorbic Ccid, Hydrocortisone, and Thiamine in Sepsis and Septic Shock - A Randomized, Double-Blind, Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
February 9, 2018 (Actual)
Primary Completion Date
November 26, 2019 (Actual)
Study Completion Date
February 28, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beth Israel Deaconess Medical Center
Collaborators
Open Philanthropy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, we aim to determine whether the combination of Ascorbic Acid (Vitamin C), Thiamine (Vitamin B1), and Corticosteroids improves the trajectory of organ failure and reduces mortality in patients with sepsis and septic shock as compared to placebo.
Detailed Description
Sepsis and Septic Shock are common and highly morbid clinical conditions without any specific therapy aside from antibiotics. A recent quasi-experimental study (Marik et. al., PMID 27940189) demonstrated a remarkable benefit when the combination of Ascorbic Acid (Vitamin C), Corticosteroids, and Thiamine (Vitamin B1) were given to patients with sepsis. In particular, patients who received this combination of medications required a shorter amount of time on vasopressors, suffered less organ failure, and had improved mortality. Vitamin C has long been suggested for treatment of patients with severe infection as it exerts significant anti-oxidant effects and reduces endothelial permeability. Corticosteroids, a mainstay of therapy for refractory shock in sepsis, have also been shown to enhance the beneficial cellular effects of vitamin C. Finally, thiamine has been shown to be an effective mitochondrial resuscitator in sepsis, especially for the ~30% of septic shock patients who present with thiamine deficiency (Donnino et. al, PMID 26771781). In this study, we aim to reproduce the findings of Marik et. al. using a more rigorous study design (i.e. a blinded, randomized clinical trial) and focus on the important clinical outcomes of organ failure and death.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Septic Shock, Metabolic Disturbance
Keywords
Sepsis, Metabolic Resuscitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
205 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin C, Vitamin B1, Corticosteroids
Arm Type
Experimental
Arm Description
The combination of vitamin C, vitamin B1, hydrocortisone : Vitamin C (ascorbic acid) 1.5g every 6 hours x 4-days Vitamin B1 (thiamine) 100mg every 6 hours x 4-days Hydrocortisone 50mg every 6 hours x 4-days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal Saline Solution (0.9%NaCl) in a volume to match all experimental arm components
Intervention Type
Drug
Intervention Name(s)
vitamin C, vitamin B1, hydrocortisone
Other Intervention Name(s)
Ascorbic Acid, Thiamine
Intervention Description
Vitamin C (1.5g) plus vitamin B1 (100mg) will be diluted in 100ml 0.9% NACL(normal saline) and administered IV every 6 hours for 4 days or until participant is discharged from the ICU. Hydrocortisone 50mg/ml will be administered via IV push over 1-2 minutes every 6hours for 4 days or until the patient is discharged from the ICU.
Intervention Type
Drug
Intervention Name(s)
Normal saline
Intervention Description
Normal saline (0.9% NaCl solution) volume to match all components
Primary Outcome Measure Information:
Title
Sequential Organ Failure Assessment (SOFA) Score at Baseline and 72 Hours
Description
Sequential Organ Failure Assessment (SOFA) Score at Baseline and 72 Hours. The SOFA score ranges from a minimum of 0 to a maximum of 24, with higher scores meaning worse outcomes.
Time Frame
Enrollment to 72-hours
Secondary Outcome Measure Information:
Title
Renal Failure
Description
Development of renal failure as defined by a Kidney Disease Improving Global Outcomes [KDIGO] stage 3 or higher. There are 3 stages in the KDIGO scale with stage 3 being the worst (corresponds to renal failure). Stage 1- serum creatinine 1.5 to 1.9 times baseline OR an increase in serum creatinine ≥ 0.3 mg/dL OR urine output < 0.5ml/kg/hour for 6-12 hours. Stage 2- serum creatinine 2.0-2.9 times baseline OR urine output <0.5mg/kg/hour for ≥ 12 hours Stage 3- serum creatinine 3.0 times baseline (or serum creatinine of more than or equal to 4.0 mg/dl with an acute increase of at least 0.5 mg/dl) (OR) Urine output less than 0.3 ml/kg/hour for 24 hours or anuria for 12 hours or new renal replacement therapy
Time Frame
Enrollment until 7-days or discharge from the ICU
Title
30-day Mortality
Description
Mortality rate
Time Frame
Enrollment until 30-days after enrollment
Other Pre-specified Outcome Measures:
Title
Ventilator Free Days
Description
Days not receiving invasive mechanical ventilation
Time Frame
Ventilator free days over the first 7-days after enrollment
Title
Shock Free Days
Description
Days not receiving vasopressor
Time Frame
Vasopressor free days over the first 7-days after enrollment
Title
ICU Free Days
Description
Number of days that the patient was not in the ICU. Timeframe listed below.
Time Frame
From enrollment until 28 days after enrollment
Title
Hospital Mortality
Description
Hospital mortality rate
Time Frame
Enrollment until hospital discharge, death, or 30-days. Whichever comes first.
Title
Intensive Care Unit (ICU) Mortality
Description
ICU mortality rate
Time Frame
Enrollment until ICU discharge, death, or 30-days. Whichever comes first.
Title
Number of Participants With Delirium
Description
Describes if patient has delirium as defined by the Confusion Assessment Method (CAM)-ICU. The CAM-ICU method requires that the patient have 3 features to qualify for delirium: Acute Onset of Changes or Fluctuations in the Course of Mental Status (AND ) Inattention (AND) Disorganized thinking (OR) Altered Level of Consciousness
Time Frame
On day 3 (at approximately 72 hours) after the first study drug dose
Title
Hospital Disposition: Survivors Discharged Home
Description
Home hospital disposition in patients who survive to discharge
Time Frame
Enrollment until hospital discharge, death, or 30-days, whichever comes first.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patient (age ≥ 18 years) Suspected (cultures drawn and antibiotic given) or confirmed (via culture results) infection Receiving vasopressor (norepinephrine, phenylephrine, epinephrine, dopamine, angiotensin II or vasopressin) Exclusion Criteria: Member of a protected population (pregnant, prisoner) Known kidney stones within the past 1 year (except for asymptomatic, incidentally noted stones on imaging) End stage renal disease (ESRD) requiring dialysis Known Glucose-6-Phosphate Dehydrogenase deficiency Known Hemachromatosis Comfort Measures Only status Anticipated death within 24-hours despite maximal therapy (as determined by the enrolling physician) Receiving supplemental thiamine in a dose greater than that contained in a multivitamin Clinical indication for steroids (e.g. chronic use) as determined by the clinical team providing this drug Clinical indication for thiamine as determined by the clinical team providing this drug Clinical indication for ascorbic acid as determined by the clinical team providing this drug Known allergy to vitamin C, hydrocortisone, or thiamine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael W Donnino, MD
Organizational Affiliation
Beth Israel Deaconess Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic - Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85054
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Mount Auburn Hospital
City
Cambridge
State/Province
Massachusetts
ZIP/Postal Code
02138
Country
United States
Facility Name
Detroit Receiving Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Harper University Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Henry Ford Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
Sinai Grace Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48235
Country
United States
Facility Name
Beaumont Hospital
City
Royal Oak
State/Province
Michigan
ZIP/Postal Code
48073
Country
United States
Facility Name
North Shore University Hospital
City
Manhasset
State/Province
New York
ZIP/Postal Code
11030
Country
United States
Facility Name
Long Island Jewish Hospital
City
New York
State/Province
New York
ZIP/Postal Code
11040
Country
United States
Facility Name
University Of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
The University of Texas Health Science Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
27940189
Citation
Marik PE, Khangoora V, Rivera R, Hooper MH, Catravas J. Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Severe Sepsis and Septic Shock: A Retrospective Before-After Study. Chest. 2017 Jun;151(6):1229-1238. doi: 10.1016/j.chest.2016.11.036. Epub 2016 Dec 6.
Results Reference
background
PubMed Identifier
28207287
Citation
Moskowitz A, Andersen LW, Cocchi MN, Karlsson M, Patel PV, Donnino MW. Thiamine as a Renal Protective Agent in Septic Shock. A Secondary Analysis of a Randomized, Double-Blind, Placebo-controlled Trial. Ann Am Thorac Soc. 2017 May;14(5):737-741. doi: 10.1513/AnnalsATS.201608-656BC.
Results Reference
background
PubMed Identifier
26771781
Citation
Donnino MW, Andersen LW, Chase M, Berg KM, Tidswell M, Giberson T, Wolfe R, Moskowitz A, Smithline H, Ngo L, Cocchi MN; Center for Resuscitation Science Research Group. Randomized, Double-Blind, Placebo-Controlled Trial of Thiamine as a Metabolic Resuscitator in Septic Shock: A Pilot Study. Crit Care Med. 2016 Feb;44(2):360-7. doi: 10.1097/CCM.0000000000001572.
Results Reference
background
PubMed Identifier
33251516
Citation
Grossestreuer AV, Moskowitz A, Andersen LW, Holmberg MJ, Konacki V, Berg KM, Chase M, Cocchi MN, Donnino MW. Effect of Ascorbic Acid, Corticosteroids, and Thiamine on Health-Related Quality of Life in Sepsis. Crit Care Explor. 2020 Nov 23;2(12):e0270. doi: 10.1097/CCE.0000000000000270. eCollection 2020 Dec.
Results Reference
derived
PubMed Identifier
32809003
Citation
Moskowitz A, Huang DT, Hou PC, Gong J, Doshi PB, Grossestreuer AV, Andersen LW, Ngo L, Sherwin RL, Berg KM, Chase M, Cocchi MN, McCannon JB, Hershey M, Hilewitz A, Korotun M, Becker LB, Otero RM, Uduman J, Sen A, Donnino MW; ACTS Clinical Trial Investigators. Effect of Ascorbic Acid, Corticosteroids, and Thiamine on Organ Injury in Septic Shock: The ACTS Randomized Clinical Trial. JAMA. 2020 Aug 18;324(7):642-650. doi: 10.1001/jama.2020.11946.
Results Reference
derived
PubMed Identifier
31852712
Citation
Moskowitz A, Yankama T, Andersen LW, Huang DT, Donnino MW, Grossestreuer AV; ACTS Clinical Trial Investigators. Ascorbic Acid, Corticosteroids and Thiamine in Sepsis (ACTS) protocol and statistical analysis plan: a prospective, multicentre, double-blind, randomised, placebo-controlled clinical trial. BMJ Open. 2019 Dec 17;9(12):e034406. doi: 10.1136/bmjopen-2019-034406.
Results Reference
derived

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Ascorbic Acid, Corticosteroids, and Thiamine in Sepsis (ACTS) Trial

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