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Effect of early adminestration of corton in sepsis

Evaluating effect of early adminestration of corticosteroid in sepsis; A randomized clinical triali

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230701058635N1
Enrollment
40
Registered
2024-02-16
Start date
2024-01-21
Completion date
Unknown
Last updated
2024-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sepsis. Systemic Inflammatory Response Syndrome of infectious origin with organ failureSevere sepsis

Interventions

Intervention 1: Concomitant with the standard of care (fluid resuscitation, antibiotic therapy, management of electrolytes and acid-base disturbances and metabolic supports) patients will receive intr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 89 Years

Inclusion criteria

Inclusion criteria: Age of 18–89 years Systolic blood pressure of 2 mmol/L SOFA score of =2 points consequent to the infection

Exclusion criteria

Exclusion criteria: Rejection of sepsis diagnosis after initial evaluations Decision to limit or withdraw treatment Steroid use within 4 weeks Chemotherapy for underlying malignancy within 4 weeks Etomidate use during hospitalization Pregnancy or lactation Informed written consent cannot be obtained from a patient or legal representative Corticosteroides contraindications

Design outcomes

Primary

MeasureTime frame
Time to enter the septic shock. Timepoint: Every 1-hour. Method of measurement: According mean artrial pressure.

Secondary

MeasureTime frame
Vasopressor requirement. Timepoint: Every 1-hour. Method of measurement: Starting a vasopressor drug (type and dose).;Need for mechanical ventilation support. Timepoint: Every 1-hour. Method of measurement: Patient intubation.;7-day mortality. Timepoint: 7 days after initial treatment. Method of measurement: patient follow-up.;28-day mortality. Timepoint: 28 days after initial treatment. Method of measurement: patient follow-up.;Length of stay in ICU. Timepoint: Daily. Method of measurement: patient follow-up.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Emami

Tehran University of Medical Sciences

e-EMAMI@student.tums.ac.ir+98 21 6670 2171

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026