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Observational study to predict the impact of proposed fluid score on organ dysfunction in a population of patients with infection.

Pocus based fluid tolerance score as a predictor of end organ dysfunction and mortality in patients with sepsis- a prospective observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/076007
Enrollment
149
Registered
2024-10-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: A419- Sepsis, unspecified organism

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Dr Arshad N N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged above 18 years, admitted to MICU with sepsis/septic shock

Exclusion criteria

Exclusion criteria: 1. Severe MR, AR 2. Pregnancy 3. Prosthetic, transplant heart

Design outcomes

Primary

MeasureTime frame
To correlate pocus based fluid tolerance score with end organ dysfunction and mortality in septic shock patients.Timepoint: Baseline, every 48 hours until ICU discharge—

Secondary

MeasureTime frame
To evaluate the incidence of organ dysfunction in adult septic patients with systemic venous congestion. Timepoint: Baseline, every 48 hours until ICU discharge—

Countries

India

Contacts

Public ContactDr Vimal Bhardwaj

Narayana Health

vmlbhardwaj@yahoo.co.in9686124830

Outcome results

None listed

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