Fludrocortisone Dose Response Relationship in Septic Shock - FluDReSS

Septic Shock Clinical Trial

— FluDReSS  

Official title:

A Phase II Open Label Randomised Controlled Clinical Trial of Different Dosing Regimens of Fludrocortisone in Septic Shock With Assessment of Temporal Changes in Hormonal, Inflammatory, and Genetic Markers of Vascular Responsiveness

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04494789
• Other study ID #: GI-CC35837377
• Status: Completed
• Phase: Phase 2
• Start date: February 11, 2021
• Est. completion date: June 30, 2023

Study information

• Verified date: January 2024
• Source: The George Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the most suitable dose of Fludrocortisone in reversal of sepsis and shock associated with sepsis in patients who are admitted to the ICU.

The investigators will be looking to see whether patients receiving Fludrocortisone at different doses recover quicker and spend less time in hospital and in ICU, and to understand the reasons why this happens at certain doses.

Sepsis is caused by toxic substances (toxins) from bacteria and other organism entering the bloodstream from a site of infection. In some people, the infection can progress to sepsis and septic shock where the functions of organs in the body are affected. Patients suffering from sepsis and septic shock are commonly managed in the intensive care unit (ICU) where they are prescribed antibiotics as standard therapy, as well as other therapies to support the functions of the body.

Fludrocortisone is a steroid that has previously shown to be beneficial to help in shock in patients in ICU, but more information is required about the exact dose that is required to achieve this. This has been shown by previous research.

However, the exact role of Fludrocortisone and the best dose has not been studied adequately to date as well as the ways in how it works within the body. The study aims to look tat the dose and the way it works.

Description:

Aim:

1. To conduct a multi-centre randomised controlled trial to assess the effect of 3 different dose regimens of fludrocortisone on shock reversal in septic shock patients treated with hydrocortisone.

2. To assess the temporal changes in endocrine inflammatory and gene expression markers in septic shock patients.

Hypotheses:

In patients with septic shock treated with hydrocortisone,

1. The addition of fludrocortisone to hydrocortisone results in improved vascular responsiveness to vasopressors as compared to hydrocortisone alone

2. The improvement of vascular responsiveness with fludrocortisone is in a dose dependent manner

3. Enterally administered fludrocortisone results in adequate plasma level

4. Patients who have early reversal of shock have higher concentrations of, angiotensin II and angiotensin II-receptor expression and reduced angiotensin converting enzyme 2 (ACE 2) concentrations at baseline and throughout the course of their illness

5. Patients who have early reversal of shock have higher concentrations of plasma free cortisol, aldosterone and glucocorticoid and mineralocorticoid receptor expression at baseline and throughout the course of their illness.

6. Patients who demonstrate evidence of both greater angiotensin II and glucocorticoid receptor expression will have earlier shock reversal than those who have an increase in expression of either of these receptors.

7. There is a different temporal change in the plasma concentrations and receptor expression profiles in early shock reversal patients vs. delayed shock reversal patients.

300 patients will be recruited and randomised to enteral doses of 50mcg fludrocortisone Q24H, Q12H, Q6H or to the control arm of the study. The study will enrol patients admitted to a participating intensive care unit and who meet all the inclusion criteria and no exclusion criteria. Patients in a fludrocortisone arm will receive enteral fludrocortisone for a maximum of 7 days or until sustained shock reversal or until discharge from ICU whichever is earlier.

Blood samples acquired will be analysed for:

• Endocrine - Cortisol, free cortisol, aldosterone and metabolites

• Inflammatory - Cytokine profiles, markers of vasoplegia

• Gene Expression - Whole genome RNA sequencing and single cell sequencing

• To assess the plasma levels following enteral administration of fludrocortisone in all patients enrolled to undertake detailed analysis of fludrocortisone kinetics in a subgroup of 30 patients enrolled (10 patients in each dosing group).

For all patients, data will be collected at baseline and daily whilst in the ICU for up to 8 days. Patients will be followed up to time of discharge from hospital or day 28 if they are still in hospital, whichever occurs first

Recruitment information / eligibility

• Status: Completed
• Enrollment: 155
• Est. completion date: June 30, 2023
• Est. primary completion date: April 30, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Aged 18 years or older

2. Documented site, or strong suspicion of infection with 2 of the 4 clinical signs of inflammation:

1. Core temperature > 38oC or < 35oC

2. Heart rate > 90bpm

3. Respiratory rate > 20bpm, or PaCO2 < 32mmHg, or mechanical ventilation

4. White cell count > 12 x 109/L or < 4 x 109/L or > 10% immature neutrophils\

3. Being treated with Hydrocortisone at a daily dose of 200mg / day as adjunctive treatment for sepsis

4. Being treated with mechanical ventilation at the time of randomisation (includes mask BiPAP/CPAP)

5. Being treated with continuous vasopressors or inotropes to maintain a systolic blood pressure > 90mmHg, or mean arterial pressure > 60mmHg or a MAP target set by the treating clinician for maintaining perfusion

6. Administration of vasopressors or inotropes for > 4 hours and present at time of randomisation

Exclusion Criteria:

1. Met all inclusion criteria more than 24 hours ago

2. Patients taking long term corticosteroids or fludrocortisone

3. Patients with systemic fungal infection

4. Death is deemed inevitable or imminent during this admission and either the attending physician, patient or surrogate legal decision maker is not committed to active treatment

5. Patient unable to receive enteral medication

6. Death from underlying disease likely within 90 days

7. Patient has been previously enrolled in the study

Related Conditions & MeSH terms

• Critical Illness
• Critically Ill
• Septic Shock
• Shock
• Shock, Septic

Intervention

Drug:
• Fludrocortisone Acetate
50mcg
• Fludrocortisone Acetate
100mcg
• Fludrocortisone Acetate
200mcg

Other:
• Standard Therapy
NO Fludrocortisone

Locations

Country	Name	City	State
Australia	Queen Elizabeth II Hospital	Adelaide	South Australia
Australia	Royal Brisbane Women's Hospital	Brisbane	Queensland
Australia	Wesley Hospital	Brisbane	Queensland
Australia	Gold Coast University Hospital	Gold Coast	Queensland
Australia	Austin Hospital	Melbourne	Victoria
Australia	Mater Misericordiae	Raymond Terrace	Queensland
Australia	Blacktown Hospital	Sydney	New South Wales
Australia	Royal North Shore Hospital	Sydney	New South Wales
Australia	Princess Alexandra Hospiital	Woolloongabba	Queensland

Sponsors (1)

Lead Sponsor	Collaborator
The George Institute

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Pharmacokinetic Outcome To assess the plasma levels of enterally administered fludrocortisone in all patients enrolled	Time to peak concentration of Fludrocortisone	7 days
Other	Pharmacokinetic Outcomes - To undertake detailed analysis of fludrocortisone kinetics in a subgroup of 30 patients enrolled (10 patients in each dosing group)	Time to absorption, clearance and metabolism of fludrocortisone in participants in each intervention arm except for the control arm	7 days
Other	Vascular Responsiveness Analysis	Acquisition of blood samples at 4 timepoints over the first 7 days or until discharge from ICU for exploratory analysis to assess a range of biomarkers and their interactions with the primary outcomes	7 days
Primary	Time to resolution of shock by Intervention group allocation	To the assess the time it takes for shock to resolve in each intervention arm	7 DAYS
Primary	Time to resolution of shock and Fludrocortisone Levels	Assess the levels of fludrocortisone in the interventional groups at time of resolution of shock	7 days
Primary	Vasopressor Responsiveness by Intervention group allocation	Area under the curve of vasopressor dose in each intervention arm	7 days
Primary	Vasopressor Responsiveness and Fludrocortisone Levels	Area under the curve of vasopressor dose associated with fludrocortisone levels	7 days
Secondary	Recurrence of shock	Time between a new episode of shock after reversal of the initial episode	censored at day 28
Secondary	Ventilation free days	Number of Days that are without ventilation during admission	censored at day 28
Secondary	ICU and hospital length of Stay	Total number of days in ICU and in hospital for the index admission	censored at day 28
Secondary	ICU and hospital mortality	The number of deaths that are recorded in participants and the location of the deaths when in hospital - ICU or ward. This will include cause of death	censored at day 28
Secondary	Delta SOFA Score	Baseline SOFA score to SOFAmax - numerical calculation based on scoring system of each participant during their admission	censored at day 28
Secondary	Maximal SOFA score	Maximum SOFA score for each participant during their admission	censored at day 28
Secondary	Superinfection	This is the number of new infections that occur >48hrs after commencing study drug	censored at day 28