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NOT YET RECRUITING
NCT07572552
PHASE2

Clinical Study Evaluating the Efficacy and Safety of Fenofibrates Versus Silymarin in Adult Patients With Sepsis

Sponsor: Tanta University

View on ClinicalTrials.gov

Summary

Sepsis is a life-threatening condition defined by organ dysfunction resulting from the body's dysregulated response to an infection (1). It begins with widespread inflammation and cellular damage, which quickly escalates into total circulatory failure and the breakdown of essential organ systems, including the lungs, kidneys, digestive tract, and brain. This study aims at evaluating the safety and efficacy of fenofibrate versus silymarin for adult patients with sepsis.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2026-05

Completion Date

2028-04

Last Updated

2026-05-07

Healthy Volunteers

No

Conditions

Interventions

DRUG

Fenofibrate

fenofibrate (145 mg) once daily plus conventional sepsis therapy for 7 days.

DRUG

Silymarin

silymarin does ranged between (980 - 1120 mg) daily, in divided doses plus conventional sepsis therapy for 7 days.