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Role of two regimens (3 vs 7 days) of corticosteroids in septic shock

Comparison of 3-Days and 7-Days Regimens of Low-dose Corticosteroids for Management of Septic Shock: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/08/002866
Enrollment
238
Registered
2012-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Septic Shock

Interventions

Intervention1: Hydrocortisone: Inj Hydrocortisone 50 mg IV 6 hourly for 3 days Control Intervention1: hydrocortisone: Inj Hydrocortisone 50 mg IV 6 hrly for 7 days

Sponsors

Post Graduate Institute of Medical Education and Research Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged more 18 years with diagnosis of refractory septic shock 2.Within 24 hour of diagnosis of sepsis/septic shock; and 3.Who give consent for participation in the study, are eligible for inclusion in the study

Exclusion criteria

Exclusion criteria: 1.Patients who are already receiving systemic corticosteroids at the time of screening. 2.Patients who require corticosteroids for longer duration such interstitial lung diseases, rheumatological diseases, exacerbation of asthma/COPD etc. 3.Immune compromised patients â?? cancers, HIV or prior history of corticosteroids use. 4.Patients who refuse to participate in the study.

Design outcomes

Primary

MeasureTime frame
Primary outcome: Overall reversal of the shock. Secondary outcomes: Reversal of shock on day-3 and day-7, in-hospital mortality, day-28 mortality, duration vasopressors requirement, and complication rates such as hyper-glycaemia, super infection and neuromuscular weakness. Timepoint: Day 3 Day 7 At the time of discharge

Secondary

MeasureTime frame
Reversal of shock on day-3 and day-7, in-hospital mortality, day-28 mortality, duration vasopressors requirement, and complication rates such as hyper-glycaemia, super infection and neuromuscular weakness. Timepoint: Day 3 Day 7 At the time of discharge

Countries

India

Contacts

Public ContactVijay HADDA

Post Graduate Institute of Medical Education and Research, Chandigarh

vijayhadda@yahoo.com919914177760

Outcome results

None listed

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