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A clinical trial to compare Inferior Vena Cava Collapsibility Index (IVCCI) and standard blood pressure monitoring as a better guide to fluid management in post spinal anaesthesia hypotension

Comparison of Inferior Vena Cava Collapsibility Index by Point of Care USG (POCUS) and Standard Haemodynamic Monitoring as a Guide to Fluid Management in Post Spinal Hypotension - A Randomised Controlled Study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055069
Enrollment
132
Registered
2023-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

None listed

Interventions

Intervention1: Fluid bolus of ringer lactate (RL) by 5ml/kg body weight of patient if IVCCI is more than 40%: Fluid bolus of ringer lactate (RL) by 5ml/kg body weight of patient if IVCCI is more than

Sponsors

Bharati Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who are undergoing infraumbilical surgery uncder central neuraxial blockade (CNB) 2. ASA I and ASA II patients 3. Patients with good IVC visualisation

Exclusion criteria

Exclusion criteria: 1. Obstetric patients 2. BMI more than 30 3. Patients with pre-existing hypovolemia 4. Patients contraindicated for central neuraxial blockade

Design outcomes

Primary

MeasureTime frame
Determination of hypotension by measuring inferior vena cava collapsibility index(IVCCI) more than 40%Timepoint: Every 15 minutes for 1 hour after induction with spinal anaesthesia—

Secondary

MeasureTime frame
Comparing the number of vasopressor doses or fluid boluses provided in case & control group to manage intra operative hypotensionTimepoint: For 1 hour post induction with spinal anaesthesia—

Countries

India

Contacts

Public ContactDr Anindya Agarwal

Bharati Hospital and Research Centre

shubhada.aphale@yahoo.com9850968630

Outcome results

None listed

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