MedPath

Measurement of blood flow time in carotid artery by ultrasound and to assess its predictability in assessing intravenous fluid response in patients admitted with hypotension

Not yet recruiting
Conditions
Other hypotension,
Registration Number
CTRI/2022/03/040761
Brief Summary

Fluids are being administered for resuscitation to increase intravascular volume thereby increasing cardiac output and blood pressure in patients admitted with hypovolemic/septic shock. Multiple methods have been recommended to assess fluid responsiveness. Measurement of changes in Corrected Carotid flow time (cCFT) is one of the non-invasive techniques to assess the changes in fluid status using bedside ultrasonography. In this study, we aim to evaluate the role of Corrected Carotid Flow Time measured by ultrasonography in predicting fluid responsiveness in patients presenting with undifferentiated shock.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

New onset Septic/Hypovolemic shock.

Exclusion Criteria
  • BMI >30 kg/m2.
  • Cardiac arrhythmia Valvular heart disease Cardiomyopathy Carotid artery stenosis COPD Symmetric anterior bilateral B lines on Lung Ultrasonography Poor transthoracic window Cardiogenic/obstructive shock Patients on vasopressor therapy.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Corrected carotid flow time as a predictor of fluid responsiveness in patients presenting with septic/hypovolemic shockBaseline | Post first fluid bolus
Secondary Outcome Measures
NameTimeMethod
Correlation between corrected Carotid flow time, Lung USG values and Stroke volume during initial fluid resuscitation of patients presenting with septic/hypovolemic shockBaseline and after each fluid bolus
Comparison of baseline variables among the responders versus non-responders to fluid resuscitationBaseline
Incidence of repeat hypotension, need of vasopressors and total fluid administered among responders versus non-responders to fluid resuscitation, in patients presenting with septic or hypovolemic shockFirst 24 hours

Trial Locations

Locations (1)

AIIMS, Rishikesh

🇮🇳

Dehradun, UTTARANCHAL, India

AIIMS, Rishikesh
🇮🇳Dehradun, UTTARANCHAL, India
Davis Cherian
Principal investigator
9843690069
cherian.davis@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.