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Effectiveness of Hour -1 sepsis bundle among cirrhosis patients with sepsis

To study effectiveness of Hour-1 sepsis bundle among cirrhosis patient with sepsis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080025
Enrollment
276
Registered
2025-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: D848- Other specified immunodeficiencies

Interventions

Intervention1: Hour-1 Sepsis Bundle: In one hour Control Intervention1: Non-Bundle Sepsis Management: The control group will receive standard sepsis management that does not follow the structured Hour

Sponsors

Datta Meghe Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18 years and older. Diagnosed with cirrhosis of the liver.

Exclusion criteria

Exclusion criteria: 1)Patients with prior liver transplantation. 2)Patients who experienced a cardiac arrest before arrival at the emergency department.

Design outcomes

Primary

MeasureTime frame
evaluated by comparing the mortality rates between patients who receive the Hour-1 Sepsis Bundle and those who receive standard sepsis care. The primary outcome will be the difference in mortality rates at a specified time (e.g., in-hospital mortality) between the intervention and control groupsTimepoint: One hour—

Secondary

MeasureTime frame
Duration of Hospital Stay, Vasopressor Use, Ventilator Use, Complications, Functional Status at Discharge Timepoint: Till discharge—

Countries

India

Contacts

Public ContactDrManikantanelakuditi

Datta Meghe Institute of Higher Education and Research

drshilpagaidhane@gmail.com7997752421

Outcome results

None listed

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