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A study to assess changes in inferior vena cava size in patients with heart failure

Not Applicable
Conditions
Health Condition 1: I509- Heart failure, unspecified
Registration Number
CTRI/2019/07/020074
Lead Sponsor
Fire
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1- Adults 18 years of age or older with NYHA Class III heart failure with any of the following in the past 12 months: a decompensation due to heart failure, heart failure treatment in a hospital day care setting or urgent outpatient heart failure visit

2- On a diuretic for the management of heart failure

3- IVC must be well visualized via Ultrasound, that is assessment of the full circumference of the IVC visible without any ambiguity

4- Written informed consent

Exclusion Criteria

1- Patients that have had deterioration in symptoms of have had a hospital admission in the previous 30 days.

2- Patients with echocardiographic evidence of severe tricupsid regurgitation

3- Significant comorbidity that would interfere with the ability to safety complete the study protocol.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To examine the normal variability of the IVC geometry in a stable group of heart failure patients. <br/ ><br> <br/ ><br>Timepoint: IVC size variability over 28 days of study period
Secondary Outcome Measures
NameTimeMethod
1.IVC area (A max and A Min) <br/ ><br>2.IVC area collapsibility <br/ ><br>3.Cardiac collapsibility and rate <br/ ><br>4.Respiration rate <br/ ><br>Timepoint: IVC size variability over 28 days of study period
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