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Early Administration of Vitamin C in Patients With Sepsis or Septic Shock in Emergency Departments: a Multicentre, Double Blinded, Randomized Controlled Trial: the C-EASIE Trial
In this clinical trial the effect of early administration of Vitamin C is investigated in patients admitted at the emergency department with sepsis or septic shock. When a patient has sepsis, his/her body is causing damage to its own tissues and organs as result of an infection. This can lead to septic shock. The patient has a low blood pressure, his/her organs stop working and the patient may even die. The aim of this trial is to investigate the efficiency of Vitamin C in sepsis and septic shock. Vitamin C is a vitamin present in various foods and has been approved as dietary supplement by the Belgian authorities. Over the years it has been proven that Vitamin C is very safe. In addition, several studies have shown that Vitamin C can also have a protective effect. It can reduce organ damage and increase survival rates. Although several studies suggest that Vitamin C can help fight sepsis, it is not yet used in practice. This Belgian trial, in which several hospitals participate, hopes to provide a clear answer to the question: "Should Vitamin C be administered to patients admitted in an emergency department with sepsis or septic shock?"
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
GasthuisZusters Antwerpen
Antwerp, Belgium
Universitair Ziekenhuis Antwerpen
Antwerp, Belgium
Centre Hospitalier Universitaire Saint-Pierre Bruxelles
Brussels, Belgium
Universitair Ziekenhuis Brussel
Brussels, Belgium
Université Libre de Bruxelles Erasme
Brussels, Belgium
Universitaire Ziekenhuizen Leuven
Leuven, Belgium
Centre Hospitalier Universitaire de Liège
Liège, Belgium
Algemeen Ziekenhuis Turnhout
Turnhout, Belgium
Start Date
June 1, 2021
Primary Completion Date
August 31, 2023
Completion Date
November 15, 2023
Last Updated
January 25, 2024
301
ACTUAL participants
Vitamin C
DRUG
Normal saline
DRUG
Lead Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
NCT04850456
NCT04955210
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07179276