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Hydrocortisone Plus Fludrocortisone in High-risk Patients Undergoing for Cardiac Surgery

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Cardiac surgery is a high-risk surgery and is associated with a rate of postoperative adverse outcomes. Like many others major surgery, cardiac surgery procedures induce a proinflammatory phase usually counterbalanced with an immunosuppressive phase so the immune response remained balanced. In some cases, the immune response might be dysregulated with a more pronounced pro inflammatory state that compromises organ perfusion and with the occurrence of organ failure. From a mechanistic approach, the relationship between organ failure is complex and multifactorial with a high level of proinflammatory cytokines, a decrease in microcirculation, an endothelial dysfunction and an activation of coagulation and over. The clinical expression is an increase in vasopressor exposure and dose, an increase in mortality and in adverse outcomes with a predominance of acute kidney injury. Various therapies have been assessed to manage cardiac surgery related sepsis including glucocorticoid therapy. Briefly, two major randomized trials assessed glucocorticoid therapy solely in scheduled cardiac surgery with cardiopulmonary bypass. No clinical benefit was demonstrated in term of reduction in postoperative mortality or adverse outcomes. Since, data support that the selection of patients at risk is crucial to demonstrate such a strategy. Indeed, data support that surprisingly some patients will have a very light immune response reflected by a low pro inflammatory cytokine. The hypothesis is that the combination glucocorticoid and fludrocortisone could decrease adverse outcomes in selected patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \> 18 years.

• Patient at intermediate/high risk (EuroSCORE II \> 4%).

• Patient admitted for scheduled cardiac surgery:

‣ Coronary artery bypass grafting (CABG).

⁃ Aortic valve replacement.

⁃ Mitral valve repair or replacement.

⁃ Surgery of the aortic root (aortic tube, Bentall procedure, Tirone David procedure, or other).

⁃ Combined surgery.

• Patient undergoing cardiopulmonary bypass (CPB).

• Informed consent signed by the patient.

Locations
Other Locations
France
CHRU Amiens
RECRUITING
Amiens
Contact Information
Primary
Christophe Beyls, MD
Beyls.christophe@chu-amiens.fr
(33)3 22 08 78 66
Time Frame
Start Date: 2025-04-30
Estimated Completion Date: 2028-06
Participants
Target number of participants: 196
Treatments
Experimental: hydrocortisone plus fludrocortisone
* Hydrocortisone 200 mg/day for 5 days or until ICU discharge, starting at the initiation of cardiopulmonary bypass (CPB), administered intravenously via syringe pump in a double-blind manner~* Fludrocortisone 50 µg/day in the morning for 5 days or until ICU discharge, administered orally or via nasogastric tube (if the patient is sedated), diluted in a glass of water, in a double-blind manner
Placebo_comparator: placebo of hydrocortisone plus fludrocortisone
* Placebo for hydrocortisone (0.9% NaCl) administered following the same protocol as fludrocortisone in the intervention group~* Placebo for fludrocortisone (capsule containing microcrystalline cellulose diluted in a glass of water) administered following the same protocol as fludrocortisone in the intervention group
Related Therapeutic Areas
Sponsors
Collaborators: University Hospital, Lille, University Hospital, Rouen
Leads: Centre Hospitalier Universitaire, Amiens

This content was sourced from clinicaltrials.gov