search
Back to results

Control of Fever in Septic Patients (COVERSEP)

Primary Purpose

Sepsis, Severe Sepsis, Septic Shock

Status
Completed
Phase
Not Applicable
Locations
Czechia
Study Type
Interventional
Intervention
Ibuprofen administration
Sponsored by
University Hospital Ostrava
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring sepsis, severe sepsis, septic shock, fever, ibuprofen, physiological reserves

Eligibility Criteria

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

Inclusion Criteria:

  • age >18 years of age
  • body temperature >38.3°C within 2 consecutive hours
  • anti-microbial therapy for a known or suspected infection

Exclusion Criteria:

  • patients admitted after successful cardiopulmonary resuscitation (CPR)
  • acute myocardial infarction
  • brain injury (traumatic and non-traumatic)
  • transfer from another ICU after 72 hours
  • pregnancy
  • antipyretic medication prior to randomization
  • non-obtaining the informed consent
  • moribund condition
  • high risk of hemodynamic or respiratory maladaptation on the metabolic effect of fever

Sites / Locations

  • University Hospital Ostrava

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Aggressive treatment strategy

Conservative treatment strategy

Arm Description

The antipyretic strategy was initiated immediately upon increase of the temperature above 38.3°C. The antipyretic strategy consisted of administration of ibuprofen (per-orally or into the nasogastric tube, or rectal administration in the form of a suppository) in therapeutical dose, alway supplemented with physical cooling in cases when the temperature exceeded 39.5°C. The body temperature was measured in the urinary bladder.

The antipyretic strategy was initiated only after the body temperature exceeded 39.5°C. The antipyretic strategy consisted of administration of ibuprofen (per-orally or into the nasogastric tube, or rectal administration in the form of a suppository) in therapeutical dose, alway supplemented with physical cooling in cases when the temperature exceeded 39.5°C. The body temperature was measured in the urinary bladder.

Outcomes

Primary Outcome Measures

SOFA score value
The SOFA score (Sequential Organ Failure Assessment) was measured on Day 3 and Day 7

Secondary Outcome Measures

Serum interleukin-6 level
The serum interleukin-6 level was measured on Day 3 and Day 7
Serum procalcitonine level
The serum procalcitonine level was measured on Day 3 and Day 7
Serum lactate level
The serum lactate level was measured on Day 3 and Day 7
Central venous oxygen saturation
The central venous oxygen saturation was measured on Day 3 and Day 7
Duration of artificial ventilation
The duration of artificial ventilation in days was observed
Duration of vasopressor support
The duration of vasopressor support in days was observed
Length of ICU stay
The length of ICU stay in days was observed
Length of hospital stay
The length of hospital stay in days was observed

Full Information

First Posted
January 10, 2020
Last Updated
January 11, 2020
Sponsor
University Hospital Ostrava
search

1. Study Identification

Unique Protocol Identification Number
NCT04227652
Brief Title
Control of Fever in Septic Patients
Acronym
COVERSEP
Official Title
Control of Fever in Septic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
September 3, 2013 (Actual)
Primary Completion Date
February 28, 2019 (Actual)
Study Completion Date
March 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Ostrava

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
The benefits of fever treatment in critically ill patients remains unclear. The aim of the prospective, randomized clinical trial was to verify the hypothesis that the administration of ibuprofen in order to decrease the fever in septic patients without limited cardiorespiratory reserve leads to decreasing their prognosis.
Detailed Description
Fever is a frequently observed part of the organism's response to infection, and it is a well-known fact that it has positive effects, as it inhibits the growth of microorganisms, and potentiates the activity of anti-microbial agents. On the other hand, fever increases the demand of tissues for oxygen and increases the production of carbon dioxide in tissues. Adapting to these metabolic changes requires an efficient cardiorespiratory apparatus. In other words, in patients with a limited cardiorespiratory reserve (typically patients of higher age or patients with a serious disease of the heart or lungs), the beneficial anti-microbial effect of fever may be masked with cardiorespiratory maladaptation to fever-induced metabolic changes. Indeed, one of the randomized clinical trials investigating the effect of "aggressive" antipyretic strategy used in practice (administration of acetaminophen at the temperature > 38.5 degrees Celsius, and addition of physical cooling should the temperature exceed 39.5 degrees Celsius upon the prognosis of critically ill patients showed that the "aggressive" treatment of fever may result in higher mortality when compared with a "permissive" approach, i.e. an approach when the treatment of fever is initiated only after the body temperature has exceeded 40 degrees Celsius. The study differs remarkably from other studies performed among the population of critically ill patients, and also from studies, which did not manifest the effect of fever treatment upon the mortality of patients, with the age of patients. The average age of patients in both arms of the study was only 47 years of age, whereas the average age of patients in other studies was usually around 60 years of age. It is thus possible to presume that, due to the lower age, the patients in this study possessed a sufficient cardiorespiratory reserve for adaptation to metabolic changes induced with fever, which may have enabled a full manifestation of its anti-microbial effect, and may have led to better patient prognosis. The mortality rate in the group of patients with the "permissive" approach to fever treatment was only 2.6 percent, whereas, in the group of patients with the "aggressive" treatment, the mortality rate was 15.9 percent (p=0.06); due to this fact, the study was prematurely terminated by the Ethics Committee. Based on this study, we decided to test the hypothesis that the administration of ibuprofen in order to decrease the fever would lead to a worsening of the patient prognosis. Ibuprofen was selected due to its potent antipyretic effect, and also due to the fact that the favorable effect of its anti-inflammatory effect upon the prognosis of patients with sepsis has not been fully demonstrated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Severe Sepsis, Septic Shock
Keywords
sepsis, severe sepsis, septic shock, fever, ibuprofen, physiological reserves

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study subjects were enrolled in two parallel groups.
Masking
None (Open Label)
Masking Description
No masking was used in the study
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Aggressive treatment strategy
Arm Type
Experimental
Arm Description
The antipyretic strategy was initiated immediately upon increase of the temperature above 38.3°C. The antipyretic strategy consisted of administration of ibuprofen (per-orally or into the nasogastric tube, or rectal administration in the form of a suppository) in therapeutical dose, alway supplemented with physical cooling in cases when the temperature exceeded 39.5°C. The body temperature was measured in the urinary bladder.
Arm Title
Conservative treatment strategy
Arm Type
Experimental
Arm Description
The antipyretic strategy was initiated only after the body temperature exceeded 39.5°C. The antipyretic strategy consisted of administration of ibuprofen (per-orally or into the nasogastric tube, or rectal administration in the form of a suppository) in therapeutical dose, alway supplemented with physical cooling in cases when the temperature exceeded 39.5°C. The body temperature was measured in the urinary bladder.
Intervention Type
Drug
Intervention Name(s)
Ibuprofen administration
Intervention Description
Administration of ibuprofen, according to treatment recommendations - per orally, into the nasogastric tube, or in the form of a suppository
Primary Outcome Measure Information:
Title
SOFA score value
Description
The SOFA score (Sequential Organ Failure Assessment) was measured on Day 3 and Day 7
Time Frame
up to 7 days
Secondary Outcome Measure Information:
Title
Serum interleukin-6 level
Description
The serum interleukin-6 level was measured on Day 3 and Day 7
Time Frame
up to 7 days
Title
Serum procalcitonine level
Description
The serum procalcitonine level was measured on Day 3 and Day 7
Time Frame
up to 7 days
Title
Serum lactate level
Description
The serum lactate level was measured on Day 3 and Day 7
Time Frame
up to 7 days
Title
Central venous oxygen saturation
Description
The central venous oxygen saturation was measured on Day 3 and Day 7
Time Frame
up to 7 days
Title
Duration of artificial ventilation
Description
The duration of artificial ventilation in days was observed
Time Frame
1 month
Title
Duration of vasopressor support
Description
The duration of vasopressor support in days was observed
Time Frame
1 month
Title
Length of ICU stay
Description
The length of ICU stay in days was observed
Time Frame
1 month
Title
Length of hospital stay
Description
The length of hospital stay in days was observed
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age >18 years of age body temperature >38.3°C within 2 consecutive hours anti-microbial therapy for a known or suspected infection Exclusion Criteria: patients admitted after successful cardiopulmonary resuscitation (CPR) acute myocardial infarction brain injury (traumatic and non-traumatic) transfer from another ICU after 72 hours pregnancy antipyretic medication prior to randomization non-obtaining the informed consent moribund condition high risk of hemodynamic or respiratory maladaptation on the metabolic effect of fever
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roman Kula, MD,CSc.
Organizational Affiliation
University Hospital Ostrava
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Ostrava
City
Ostrava
State/Province
Moravian-Silesian Region
ZIP/Postal Code
70852
Country
Czechia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There exists no plan to make individual participant data available to other researchers.
Citations:
PubMed Identifier
16433601
Citation
Schulman CI, Namias N, Doherty J, Manning RJ, Li P, Elhaddad A, Lasko D, Amortegui J, Dy CJ, Dlugasch L, Baracco G, Cohn SM. The effect of antipyretic therapy upon outcomes in critically ill patients: a randomized, prospective study. Surg Infect (Larchmt). 2005 Winter;6(4):369-75. doi: 10.1089/sur.2005.6.369. Erratum In: Surg Infect (Larchmt). 2010 Oct;11(5):495. Li, Pam [corrected to Li, Pamela]; Alhaddad, Ahmed [corrected to Elhaddad, Ahmed].
Results Reference
background
PubMed Identifier
26436473
Citation
Young P, Saxena M, Bellomo R, Freebairn R, Hammond N, van Haren F, Holliday M, Henderson S, Mackle D, McArthur C, McGuinness S, Myburgh J, Weatherall M, Webb S, Beasley R; HEAT Investigators; Australian and New Zealand Intensive Care Society Clinical Trials Group. Acetaminophen for Fever in Critically Ill Patients with Suspected Infection. N Engl J Med. 2015 Dec 3;373(23):2215-24. doi: 10.1056/NEJMoa1508375. Epub 2015 Oct 5.
Results Reference
background
PubMed Identifier
28386165
Citation
Ye S, Xu D, Zhang C, Li M, Zhang Y. Effect of Antipyretic Therapy on Mortality in Critically Ill Patients with Sepsis Receiving Mechanical Ventilation Treatment. Can Respir J. 2017;2017:3087505. doi: 10.1155/2017/3087505. Epub 2017 Mar 12.
Results Reference
background
PubMed Identifier
9070471
Citation
Bernard GR, Wheeler AP, Russell JA, Schein R, Summer WR, Steinberg KP, Fulkerson WJ, Wright PE, Christman BW, Dupont WD, Higgins SB, Swindell BB. The effects of ibuprofen on the physiology and survival of patients with sepsis. The Ibuprofen in Sepsis Study Group. N Engl J Med. 1997 Mar 27;336(13):912-8. doi: 10.1056/NEJM199703273361303.
Results Reference
background

Learn more about this trial

Control of Fever in Septic Patients

We'll reach out to this number within 24 hrs