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A study to assess the usefulness of measuring blood flow time in the femoral artery for deciding the need of fluid therapy in adult patients with septic shock

Validation of pressure transducer derived femoral artery corrected flow time for volume responsiveness in adult patients with septic shock - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/078792
Enrollment
30
Registered
2024-12-31
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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 Control Intervention2: Nil: Nil

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosis of septic shock, with femoral arterial catheter and central venous catheter inserted for hemodynamic management and monitoring

Exclusion criteria

Exclusion criteria: Refusal to participate Pregnancy

Design outcomes

Primary

MeasureTime frame
To identify the diagnostic ability femoral artery corrected flow time to predict volume responsiveness defined by an increase in cardiac output by more than 10% with passive leg raise test Timepoint: within first 72 hours of developing septic shock—

Secondary

MeasureTime frame
1.To develop a predictive equation to estimate cardiac output from corrected flow time and other hemodynamic data. 2. To know the diagnostic ability of change in femoral artery corrected flow time after passive leg raise to predict volume responsiveness.Timepoint: within first 72 hours of developing septic shock—

Countries

India

Contacts

Public ContactDr Sulagna Bhattacharjee

AIIMS, New Delhi

bhattacharjee.sulagna85@gmail.com01126593212

Outcome results

None listed

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