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Not Yet RecruitingNCT07313670

Outcome of Using Hydrocortisone in Early Treatment of Pediatric Septic Shock

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
122 (estimated)
Sponsor
Muhammad Aamir Latif · Academic / Other
Sex
All
Age
2 Months – 12 Years
Healthy volunteers
Not accepted

Summary

Although, hydrocortisone has shown promise in managing refractory shock, its role in early septic shock management remains unclear. This study aims to provide robust evidence on the clinical and hemodynamic outcomes of early hydrocortisone use in pediatric septic shock, contributing to standardized treatment protocols and improved survival rates.

Detailed description

Despite global advancements in pediatric critical care, mortality and morbidity in septic shock remain unacceptably high. Although data suggest a reduction in mortality with steroid therapy in refractory shock, specific data for hydrocortisone in pediatrics are limited. The findings of this study would not only be a valuable addition to the existing stats but might also help develop a protocol for the use of hydrocortisone therapy in children with septic shock, seeking an earlier recovery from organ failure, earlier reversal of shock, and lower mortality in children with sepsis and septic shock.

Conditions

Interventions

TypeNameDescription
DRUGIntravenous HydrocortisoneChildren will receive early intravenous hydrocortisone at 2 mg/kg/day divided every 6 hours, continued for 7 days or until resolution of shock.
DRUGStandard careThe children will be managed by following standard institutional treatment protocol.

Timeline

Start date
2026-01-01
Primary completion
2026-06-30
Completion
2026-06-30
First posted
2026-01-02
Last updated
2026-01-02

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT07313670. Inclusion in this directory is not an endorsement.