Safety and Efficacy of Early Administration of Dexamethasone in High-risk Sepsis

NCT05136560 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2025-05-31

No results posted yet for this study

Summary

The purpose of this study is to investigate the safety and efficacy of early administration of two different doses of dexamethasone in high risk septic patients.

Conditions

Interventions

DRUG

Dexamethasone

Intervention drugs would be administered for 1 or 2 days.

Sponsors & Collaborators

  • CHA University

    lead OTHER

Principal Investigators

  • Kyuseok Kim, M.D, PhD · Bundang CHA Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-15
Primary Completion
2025-12-30
Completion
2026-02-28

Countries

  • South Korea

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05136560 on ClinicalTrials.gov