Clinical Trials Directory

Trials / Completed

CompletedNCT06537180

Gender-based Differences in the Outcome of the Treatment of Persistent Septic Shock With Hydrocortisone

Status
Completed
Phase
Study type
Observational
Enrollment
621 (actual)
Sponsor
Alexandria University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to explore the gender-based differences in the outcomes of treatment with hydrocortisone in critically ill patients with persistent septic shock.

Detailed description

Because of their pleiotropic effects, corticosteroids are widely used as adjunctive therapy in sepsis for their anti-inflammatory, metabolic, and immune-suppressing actions. Moreover, the treatment benefits of corticosteroids in terms of hemodynamics and organ functions for septic shock were established. Hydrocortisone reduces the duration of mechanical ventilation and critical care treatment and reduces the time needed for shock reversal. Hydrocortisone use at a daily dose of ≤400 mg for at least 3 days was associated with survival benefits. Interestingly, corticosteroid treatment was reported to be more cost-effective in females than in males with septic shock, compared with placebo. This may be explained by the fact that sex hormones modulate the expression and sensitivity of glucocorticoid receptors differently, potentially influencing the body's response to cortisol. To the best of our knowledge, the data available on whether females and males may be more or less likely to acquire a better or worse prognosis of persistent septic shock when treated with hydrocortisone is sparse. The aim of this study is to explore the gender-based differences in the outcomes of treatment with hydrocortisone in critically ill patients with persistent septic shock.

Conditions

Timeline

Start date
2023-01-01
Primary completion
2023-07-30
Completion
2024-08-01
First posted
2024-08-05
Last updated
2024-08-06

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06537180. Inclusion in this directory is not an endorsement.