Skip to main content
OpenTrials
Completed

NCT Number: NCT04227652

Control of Fever in Septic Patients

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Ostrava

Ostrava, Moravian-Silesian Region, 70852, Czechia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Ibuprofen administration

Drug

Administration of ibuprofen, according to treatment recommendations - per orally, into the nasogastric tube, or in the form of a suppository

Primary outcomes

  1. SOFA score value

    Time frame: up to 7 days

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

Secondary outcomes

  1. Serum interleukin-6 level

    Time frame: up to 7 days

    The serum interleukin-6 level was measured on Day 3 and Day 7

  2. Serum procalcitonine level

    Time frame: up to 7 days

    The serum procalcitonine level was measured on Day 3 and Day 7

  3. Serum lactate level

    Time frame: up to 7 days

    The serum lactate level was measured on Day 3 and Day 7

  4. Central venous oxygen saturation

    Time frame: up to 7 days

    The central venous oxygen saturation was measured on Day 3 and Day 7

  5. Duration of artificial ventilation

    Time frame: 1 month

    The duration of artificial ventilation in days was observed

  6. Duration of vasopressor support

    Time frame: 1 month

    The duration of vasopressor support in days was observed

  7. Length of ICU stay

    Time frame: 1 month

    The length of ICU stay in days was observed

  8. Length of hospital stay

    Time frame: 3 months

    The length of hospital stay in days was observed

Sponsors and collaborators

Lead sponsor

University Hospital Ostrava

Other

Registry information

Acronym: COVERSEP

Important dates

Study start
2013
Primary completion
2019
Study completion
2019
First posted
Jan 13, 2020
Registry last updated
Jan 14, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.