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Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock (HYVCTTSSS)

Primary Purpose

Sepsis

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Hydrocortisone, Vitamin C, and Thiamine
Normal saline
Sponsored by
Zhujiang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring corticosteroid, hydrocortisone, septic shock, thiamine, vitamin C

Eligibility Criteria

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

Inclusion Criteria:

  • A primary diagnosis of sepsis or septic shock (the diagnoses of sepsis and septic shock are based on the 2016 the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)) and a procalcitonin (PCT) level≥2ng/mL.

Sepsis: Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection.

Septic shock: Septic shock is a subset of sepsis in which underlying circulatory and cellular/metabolic abnormalities are profound enough to substantially increase mortality.

Exclusion Criteria:

  • Patients < 18 years of age, pregnant patients, and patients with limitations of care.

Sites / Locations

  • Department of Critical Care Medicine of Zhujiang Hospital,Southern Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

vitamin C、hydrocortisone、thiamine

normal saline

Arm Description

Intravenous vitamin C (1.5 g every 6 h for 4 days or until ICU discharge), hydrocortisone (50 mg every 6 h for 7 days or until ICU discharge followed by a taper over 3 days), as well as intravenous thiamine (200 mg every 12 h for 4 days or until ICU discharge).

Normal saline 500ml every day for 4 days,then 200ml every day for 3 days.

Outcomes

Primary Outcome Measures

hospital survival

Secondary Outcome Measures

duration of vasopressor therapy
requirement for renal replacement therapy in participants with Acute kidney injury(AKI)
ICU length of stay(LOS)
the change in serum procalcitonin (PCT)
Sepsis-Related Organ Failure Assessment(SOFA)score

Full Information

First Posted
August 15, 2017
Last Updated
March 10, 2019
Sponsor
Zhujiang Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03258684
Brief Title
Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock
Acronym
HYVCTTSSS
Official Title
Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock: A Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
September 25, 2017 (Actual)
Primary Completion Date
February 2, 2019 (Actual)
Study Completion Date
February 2, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhujiang Hospital

4. Oversight

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

5. Study Description

Brief Summary
In this prospective clinical study, the investigators compare the outcome and clinical course of consecutive septic participants treated with intravenous vitamin C, hydrocortisone, and thiamine (treatment group) with a control group treated in the investigators' ICU. The primary outcome is hospital survival. A propensity score is generated to adjust the primary outcome.There is 70 participants in each group.
Detailed Description
A prospective randomized controlled trial is conducted.One hundred and forty severe sepsis or septic shock participants admit to the Department of Critical Care Medicine of Zhujiang Hospital,Southern Medical University from September 2017.The participants are divided into control group ( n = 70 ) and treatment group ( n = 70 ).The participants in both groups are treated according to "2016 international guidelines for management of sepsis and septic shock",and the participants in treatment group receive intravenous vitamin C, hydrocortisone, and thiamine. The participants in control group receive normal saline.The patients' clinical and demographic data, including age, sex, admitting diagnosis, comorbidities, requirement for mechanical ventilation, use of vasopressors, daily urine output, fluid balance after 24 and 72 h, length of ICU stay (LOS),and laboratory data (serum creatinine, White Blood Cell (WBC), platelet count, total bilirubin, procalcitonin(PCT), and lactate levels), are recorded.The primary outcome is hospital survival. Secondary outcomes include duration of vasopressor therapy,requirement for renal replacement therapy in patients with Acute kidney injury (AKI), ICU LOS, and the change in serum procalcitonin and Sepsis-Related Organ Failure Assessment (SOFA score) over the first 72 h. Summary statistics are used to describe the clinical data and are presented as means±SD, medians and interquartile range, or percentages as appropriate.Statistical analysis is performed with NCSS 11 (NCSS Statistical Software) and SPSS Statistics version 24 (IBM).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis
Keywords
corticosteroid, hydrocortisone, septic shock, thiamine, vitamin C

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The participants in treatment group receive intravenous vitamin C, hydrocortisone, and thiamine. The participants in control group receive normal saline.
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
vitamin C、hydrocortisone、thiamine
Arm Type
Active Comparator
Arm Description
Intravenous vitamin C (1.5 g every 6 h for 4 days or until ICU discharge), hydrocortisone (50 mg every 6 h for 7 days or until ICU discharge followed by a taper over 3 days), as well as intravenous thiamine (200 mg every 12 h for 4 days or until ICU discharge).
Arm Title
normal saline
Arm Type
Placebo Comparator
Arm Description
Normal saline 500ml every day for 4 days,then 200ml every day for 3 days.
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone, Vitamin C, and Thiamine
Intervention Description
Intervention
Intervention Type
Other
Intervention Name(s)
Normal saline
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
hospital survival
Time Frame
Up to Day 14
Secondary Outcome Measure Information:
Title
duration of vasopressor therapy
Time Frame
Up to hour 72
Title
requirement for renal replacement therapy in participants with Acute kidney injury(AKI)
Time Frame
Up to Day 14
Title
ICU length of stay(LOS)
Time Frame
Up to Day 14
Title
the change in serum procalcitonin (PCT)
Time Frame
Up to hour 72
Title
Sepsis-Related Organ Failure Assessment(SOFA)score
Time Frame
Up to hour 96

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A primary diagnosis of sepsis or septic shock (the diagnoses of sepsis and septic shock are based on the 2016 the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)) and a procalcitonin (PCT) level≥2ng/mL. Sepsis: Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection. Septic shock: Septic shock is a subset of sepsis in which underlying circulatory and cellular/metabolic abnormalities are profound enough to substantially increase mortality. Exclusion Criteria: Patients < 18 years of age, pregnant patients, and patients with limitations of care.
Facility Information:
Facility Name
Department of Critical Care Medicine of Zhujiang Hospital,Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510282
Country
China

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
32243943
Citation
Chang P, Liao Y, Guan J, Guo Y, Zhao M, Hu J, Zhou J, Wang H, Cen Z, Tang Y, Liu Z. Combined Treatment With Hydrocortisone, Vitamin C, and Thiamine for Sepsis and Septic Shock: A Randomized Controlled Trial. Chest. 2020 Jul;158(1):174-182. doi: 10.1016/j.chest.2020.02.065. Epub 2020 Mar 31.
Results Reference
derived
Links:
URL
http://dx.doi.org/10.1016/j.chest.2016.11.036
Description
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Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock

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